| SNP - dbSNP |
| dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
| rs346807 | snp | C/T | 0.185788 | 0.241613 | intron-variant | UBE2O | GRCh38.p7 | 17:76411964 | CTGGGATTACAGGCG[C/T]GAGCCACTGTGCCTG | 63893 |
| rs346808 | snp | A/G | 0.179105 | 0.239737 | intron-variant | UBE2O | GRCh38.p7 | 17:76409204 | cgatctcctgacctc[A/G]tgatctgccagcctc | 63893 |
| rs346809 | snp | A/G | 0.171057 | 0.237209 | intron-variant | UBE2O | GRCh38.p7 | 17:76409198 | tgctctcgatctcct[A/G]acctcgtgatctgcc | 63893 |
| rs346810 | snp | A/G | 0.179105 | 0.239737 | intron-variant | UBE2O | GRCh38.p7 | 17:76409032 | ggagtgcagtggcgc[A/G]atctcggctcactgc | 63893 |
| rs346811 | snp | C/T | 0.171057 | 0.237209 | intron-variant | UBE2O | GRCh38.p7 | 17:76407844 | AACAGCAGCTCCACC[C/T]CACCAGGATGCTGCC | 63893 |
| rs346816 | snp | C/T | 0.182296 | 0.240658 | intron-variant | UBE2O | GRCh38.p7 | 17:76394857 | AAATTAATTATATTA[C/T]GATTACTCCTCAAGC | 63893 |
| rs346817 | snp | C/T | 0.125269 | 0.216661 | intron-variant | UBE2O | GRCh38.p7 | 17:76400405 | AGCAACCCAGGGGCA[C/T]GCGTGGGACAGGGCT | 63893 |
| rs369654 | snp | C/T | 0.179105 | 0.239737 | intron-variant | UBE2O | GRCh38.p7 | 17:76420065 | CCACAGCTCATGATC[C/T]GGAGCCTCACCCCTA | 63893 |
| rs372126 | snp | A/G | 0.251578 | 0.249995 | intron-variant | UBE2O | GRCh38.p7 | 17:76417134 | GGCCCTTCCGGCTAC[A/G]GCTCCAGAGCTTGTC | 63893 |
| rs372558 | snp | C/G | 0.498908 | 0.0233371 | intron-variant | UBE2O | GRCh38.p7 | 17:76422094 | TGGTGATGTTTTTGA[C/G]ACCTCTATGTGTGAT | 63893 |
| rs377253 | snp | C/G | 0.179744 | 0.239925 | intron-variant | UBE2O | GRCh38.p7 | 17:76417073 | CCCCTGATGAGGCAT[C/G]TGGTGCCCAGAGATG | 63893 |
| rs381774 | snp | A/G | 0.178785 | 0.239642 | intron-variant | UBE2O | GRCh38.p7 | 17:76415706 | GCTACTTAGGAGGCC[A/G]AGGTAGGAGAATTGC | 63893 |
| rs389809 | snp | A/G | 0.0829062 | 0.185956 | intron-variant | UBE2O | GRCh38.p7 | 17:76417915 | AGGACTCAAATACCA[A/G]CGGAAACAGCACCAT | 63893 |
| rs394873 | snp | A/G | 0.499897 | 0.00718776 | intron-variant | UBE2O | GRCh38.p7 | 17:76417367 | TTCCCTGGAGAAGAC[A/G]ATAACATTTACAAAG | 63893 |
| rs404014 | snp | G/T | 0.0836354 | 0.186609 | intron-variant | UBE2O | GRCh38.p7 | 17:76418204 | CAGCCTTCTGACAAT[G/T]TTTTCTATACTATTA | 63893 |
| rs423130 | snp | C/T | 0.172674 | 0.237741 | intron-variant | UBE2O | GRCh38.p7 | 17:76420107 | TTTGGGGGAGTGTGG[C/T]GCGAAGGGGGCCACT | 63893 |
| rs435892 | snp | A/T | 0.17332 | 0.23795 | intron-variant | UBE2O | GRCh38.p7 | 17:76402424 | ATCTGCCGTGGCCTA[A/T]TTCTGTTGCTCAGTT | 63893 |
| rs443112 | snp | A/G | 0.179744 | 0.239925 | intron-variant | UBE2O | GRCh38.p7 | 17:76417817 | CATGGATGCATCAGC[A/G]TCCGCGAAGAGACGT | 63893 |
| rs444896 | snp | A/G | 0.180064 | 0.240019 | intron-variant | UBE2O | GRCh38.p7 | 17:76425254 | AAAAAAAAAAAAGTA[A/G]AAGAAAAAAATGTGG | 63893 |
| rs445683 | snp | A/G | 0.499965 | 0.00419314 | intron-variant | UBE2O | GRCh38.p7 | 17:76405440 | GAGCCTGCCCACCTC[A/G]CACTCTGCATGTGGG | 63893 |
| rs447921 | snp | A/G | 0.219049 | 0.248077 | intron-variant | UBE2O | GRCh38.p7 | 17:76418477 | TGAATTGAATATCTA[A/G]ACTTCCTCCAACTGT | 63893 |
| rs452868 | snp | A/C | 0.17332 | 0.23795 | intron-variant | UBE2O | GRCh38.p7 | 17:76425401 | aaggcttaacaaaaa[A/C]aggcagtcccccatc | 63893 |
| rs453116 | snp | G/T | 0.179425 | 0.239831 | intron-variant | UBE2O | GRCh38.p7 | 17:76405722 | GCTGGTCGGAGGTGT[G/T]TGCGGTCTGTGAAGA | 63893 |
| rs454879 | snp | A/C | 0.375 | 0.216506 | intron-variant | UBE2O | GRCh38.p7 | 17:76418574 | TCAAAAAAAAAAAAA[A/C]AAAACCTGTTCCTCC | 63893 |
| rs493035 | snp | A/G | 0.179105 | 0.239737 | intron-variant | UBE2O | GRCh38.p7 | 17:76445075 | AGCAGCTCCGATGAT[A/G]TTCTTCCTCCTCCTT | 63893 |
| rs495055 | snp | C/T | 0.179425 | 0.239831 | intron-variant | UBE2O | GRCh38.p7 | 17:76444808 | TTATTTAAGGGATTC[C/T]GAGGGCCCTGAAGGT | 63893 |
| rs500466 | snp | A/T | 0.375 | 0.216506 | intron-variant | UBE2O | GRCh38.p7 | 17:76434794 | TTTGTTTGTTTTTTT[A/T]AAAAAAAAAAAAAAA | 63893 |
| rs546588 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | UBE2O | GRCh38.p7 | 17:76435803 | GACAGGCTGGTCTGT[C/T]GTGCCTTCAGCTCAG | 63893 |
| rs560924 | snp | A/G | 0.178785 | 0.239642 | intron-variant | UBE2O | GRCh38.p7 | 17:76420349 | GCTATGGAGGAGCAG[A/G]GGGCTATGGAAGTGC | 63893 |
| rs567009 | snp | C/T | 0.483491 | 0.0893421 | intron-variant | UBE2O | GRCh38.p7 | 17:76438735 | GAAACACTGGTTATG[C/T]TGGTCTTACTGATGG | 63893 |
| rs568020 | snp | C/T | 0.14933 | 0.228835 | intron-variant | UBE2O | GRCh38.p7 | 17:76438612 | AGAACAGTAATAAAG[C/T]TTTCAATTATTAGAG | 63893 |
| rs579983 | snp | A/T | 0.100944 | 0.200705 | intron-variant | UBE2O | GRCh38.p7 | 17:76442459 | CCTCCCACTTACTAC[A/T]AATAGTATTCTTAGT | 63893 |
| rs619907 | snp | C/T | 0.179425 | 0.239831 | intron-variant | UBE2O | GRCh38.p7 | 17:76449694 | TGACCTCAGGTGATC[C/T]GCCCGCCTCGGCCTC | 63893 |
| rs669228 | snp | A/G | 0.0228947 | 0.104514 | intron-variant | UBE2O | GRCh38.p7 | 17:76441530 | GTACGTCTTTGGTTC[A/G]AGGCTTTTTCTCTCC | 63893 |
| rs679396 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | UBE2O | GRCh38.p7 | 17:76445228 | GACTGCCTTTTTTTT[C/T]TTCTTTTTCCAAGCA | 63893 |
| rs694251 | snp | C/T | 0.0364509 | 0.129988 | intron-variant | UBE2O | GRCh38.p7 | 17:76442857 | CCTGCACTGTGTAGC[C/T]TTCTCCCTGGTCTCC | 63893 |
| rs898083 | snp | A/G | 0.499913 | 0.00658888 | intron-variant | UBE2O | GRCh38.p7 | 17:76416202 | TGTATATGTGTATAT[A/G]TGTGTGTATATGTAT | 63893 |
| rs898084 | snp | G/T | 0.185311 | 0.241486 | downstream-variant-500B | UBE2O | GRCh38.p7 | 17:76389510 | TTTTTTTTTTTTTTT[G/T]TGTTGGCTCATTAGC | 63893 |
| rs898085 | snp | A/G | 0.427727 | 0.175821 | intron-variant | UBE2O | GRCh38.p7 | 17:76397600 | TCGCTTCTCCCAGCA[A/G]TCTCTTCACGTCCAT | 63893 |
| rs1000820 | snp | C/T | 0.121022 | 0.21416 | intron-variant | UBE2O | GRCh38.p7 | 17:76437641 | GCTGGCCTTGAACTC[C/T]TGGACCCAAGCGATC | 63893 |
| rs1000821 | snp | C/T | 0.378765 | 0.214288 | intron-variant | UBE2O | GRCh38.p7 | 17:76437921 | AAGGAAGATGGGGGA[C/T]AGGCTAAATACACGC | 63893 |
| rs1254663 | snp | C/T | 0.0182019 | 0.0936463 | intron-variant | UBE2O | GRCh38.p7 | 17:76437461 | tttttctttttcttt[C/T]tttttttttttgaga | 63893 |
| rs1356533 | snp | G/T | 0.481009 | 0.0955756 | intron-variant | UBE2O | GRCh38.p7 | 17:76447872 | AGGCACAGGGCTGGC[G/T]CTCTCTGACAGACAT | 63893 |
| rs1356534 | snp | A/G | 0 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76427634 | TTGTTCTGCAAGCAA[A/G]AAGCTTCAGGGGTAT | 63893 |
| rs1466003 | snp | A/G | 0.422787 | 0.180679 | intron-variant | UBE2O | GRCh38.p7 | 17:76439277 | AGGACTGTAAATAAC[A/G]ATAACAACAAAGGTT | 63893 |
| rs1533570 | snp | C/T | 0.477345 | 0.103991 | intron-variant | UBE2O | GRCh38.p7 | 17:76425895 | TTCCTCTGCCGCTCA[C/T]CTGTGTCAGATCCCG | 63893 |
| rs1550767 | snp | A/G | 0.079617 | 0.182947 | intron-variant | UBE2O | GRCh38.p7 | 17:76432281 | TGGATTGACAGGAAC[A/G]TACTTTGATAACTGA | 63893 |
| rs1674350 | snp | A/G | 0.180064 | 0.240019 | intron-variant | UBE2O | GRCh38.p7 | 17:76416115 | TGCGTATGTGTATAC[A/G]TATATACATATATGT | 63893 |
| rs1811459 | snp | C/T | 0.100944 | 0.200705 | intron-variant | UBE2O | GRCh38.p7 | 17:76443610 | CCCAAGTCTGTGGAC[C/T]TAAAAAAAAAAAAAT | 63893 |
| rs1811460 | snp | A/C | 0.497933 | 0.032082 | intron-variant | UBE2O | GRCh38.p7 | 17:76443601 | GTGGACTTAAAAAAA[A/C]AAAAAATGTTCTGAC | 63893 |
| rs1899996 | snp | A/C | 0.00438332 | 0.0466095 | | | GRCh38.p7 | 17:76443879 | TACCAGACTATACCA[A/C]ATGTTTCTCTTTTTT | 63893 |
| rs1968767 | snp | A/T | 0.475081 | 0.108804 | intron-variant | UBE2O | GRCh38.p7 | 17:76424862 | TTCTttttttttttt[A/T]attttttattttttt | 63893 |
| rs2009584 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76435417 | TGTGTGTGTGTGTGT[A/G]TGTGTGTGTGTGTGT | 63893 |
| rs2958219 | snp | C/T | 0 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76406744 | CCATTGCACTCCAGT[C/T]TGGGCAACACAGCGA | 63893 |
| rs3135933 | snp | A/G | 0.497558 | 0.0348586 | intron-variant | UBE2O | GRCh38.p7 | 17:76449709 | GGATCACCTGAGGTC[A/G]GGAGTTCAAGAACAG | 63893 |
| rs3219583 | microsatellite | (CA)19/20/21/22/23/24/25/26/27/30/31/32 | 0.83205 | 0.110663 | intron-variant | UBE2O | GRCh38.p7 | 17:76435403 | TTAAATATACAGATA[lengthTooLong]AAAGATTAAGATTTA | 63893 |
| rs3744042 | snp | A/C | 0 | 0 | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390300 | TGGGCGTCACCCGGA[A/C]CCTAGCCTGGTCCCA | 63893 |
| rs3744043 | snp | A/G | 0.0690024 | 0.172453 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76398853 | TCGCTTATCTACCAC[A/G]AAGTCTCCAGGGCAG | 63893 |
| rs3803739 | snp | C/T | 0.497671 | 0.0340435 | missense | UBE2O | GRCh38.p7 | 17:76391203 | TAGCTGAGGCCAGGC[C/T]CTGGGCACCGCCCTC | 63893 |
| rs3809691 | snp | C/G | 0.39457 | 0.203972 | intron-variant | UBE2O | GRCh38.p7 | 17:76400340 | TGGGCTGGACTCCTG[C/G]GAGGCCAGCAGTGTT | 63893 |
| rs3809693 | snp | A/G | 0.453939 | 0.144598 | intron-variant | UBE2O | GRCh38.p7 | 17:76400945 | GCAGGAAGGAAAGGG[A/G]CAGCAGCTCAGCTCC | 63893 |
| rs3833087 | in-del | -/C | | | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390543 | TTGTTGGCGCAACCC[-/C]ACACTTCATGCAAGG | 63893 |
| rs4238986 | snp | A/G | 0.475789 | 0.107327 | intron-variant | UBE2O | GRCh38.p7 | 17:76415995 | catatgcacatacac[A/G]tatatacgtatgtgt | 63893 |
| rs4238987 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76432004 | AGGCATGGATAAATC[A/C]ACACTTTACACACTC | 63893 |
| rs4419085 | snp | C/T | 0.170408 | 0.236992 | intron-variant | UBE2O | GRCh38.p7 | 17:76447601 | CCCCCTCCTGGAGGA[C/T]GGCCGGGGTTACTTT | 63893 |
| rs4422008 | snp | A/T | 0.488374 | 0.075352 | intron-variant | UBE2O | GRCh38.p7 | 17:76443295 | GGAATATATATATAT[A/T]TTTTTTTCCTCGAGA | 63893 |
| rs4458029 | snp | A/G | 0.47709 | 0.104548 | intron-variant | UBE2O | GRCh38.p7 | 17:76415935 | catacacgtatatac[A/G]tatgcgtatacatat | 63893 |
| rs4462625 | snp | A/G | 0.499937 | 0.0055907 | intron-variant | UBE2O | GRCh38.p7 | 17:76416744 | TCACTTCTTGGCTGG[A/G]TCATTAGGTCCTAAG | 63893 |
| rs4516263 | snp | C/T | 0.489259 | 0.0724914 | intron-variant | UBE2O | GRCh38.p7 | 17:76436480 | CCAGCAATTTTTCTT[C/T]GGTGCTGGATTGTCA | 63893 |
| rs4550478 | snp | C/T | 0.499902 | 0.00698814 | intron-variant | UBE2O | GRCh38.p7 | 17:76416736 | CCAAAATGTCACTTC[C/T]TGGCTGGGTCATTAG | 63893 |
| rs4789291 | snp | G/T | 0.477684 | 0.103247 | intron-variant | UBE2O | GRCh38.p7 | 17:76410046 | TTACCAAGCAGGGAG[G/T]AGTAGCTGTCAAGGT | 63893 |
| rs4789294 | snp | A/G | 0.471673 | 0.115589 | intron-variant | UBE2O | GRCh38.p7 | 17:76423095 | GGAGAACATCTGGCA[A/G]TGCAGGAAACAGGAA | 63893 |
| rs4789295 | snp | A/C | 0.471578 | 0.115772 | intron-variant | UBE2O | GRCh38.p7 | 17:76423098 | GAACATCTGGCAATG[A/C]AGGAAACAGGAATCA | 63893 |
| rs4789296 | snp | C/T | 0.485118 | 0.0849685 | intron-variant | UBE2O | GRCh38.p7 | 17:76444468 | CTTGAGCCCAGGAGG[C/T]GGAGGCTGCAGTAAG | 63893 |
| rs4789297 | snp | A/C | 0.171057 | 0.237209 | intron-variant | UBE2O | GRCh38.p7 | 17:76451269 | CAATAACCCTCTTTT[A/C]CTGACACAATACTGG | 63893 |
| rs4789298 | snp | C/T | 0.482008 | 0.0931261 | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76453976 | ATTAACTTATTTTCA[C/T]CTTAATTTGCTCATC | 63893 |
| rs5822131 | in-del | -/ACTA | 0.17332 | 0.23795 | intron-variant | UBE2O | GRCh38.p7 | 17:76431652 | GGAAAAGAAAGACTA[-/ACTA]TTAGGGCCAGACACT | 63893 |
| rs5822133 | in-del | -/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76441043 | TTGAATTTGGGTTGG[-/C]CTCCCACTTGCTATG | 63893 |
| rs5822135 | in-del | -/T | 0.497933 | 0.032082 | intron-variant | UBE2O | GRCh38.p7 | 17:76443595 | TGCCCAGTCAGAACA[-/T]TTTTTTTTTTTTTAA | 63893 |
| rs7207108 | snp | A/G | 0.465263 | 0.127129 | intron-variant | UBE2O | GRCh38.p7 | 17:76417803 | GGTGTTTGATGCTGC[A/G]TGGATGCATCAGCGT | 63893 |
| rs7207792 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | UBE2O | GRCh38.p7 | 17:76442157 | CCAGCTCTAGCTAGC[C/T]CTAGCCTAGTCCACA | 63893 |
| rs7207983 | snp | G/T | 0.427119 | 0.176434 | intron-variant | UBE2O | GRCh38.p7 | 17:76434992 | ATGGCAGAGCTGGGC[G/T]CTCCCTGCAGTGGCA | 63893 |
| rs7209271 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76394863 | GGAGTAATCATAATA[C/T]AATTAATTTCAAAGT | 63893 |
| rs7209978 | snp | A/G | 0.130008 | 0.219321 | intron-variant | UBE2O | GRCh38.p7 | 17:76444793 | AAGATGATGTCATCA[A/G]CCTTCAGGGCCCTCA | 63893 |
| rs7210520 | snp | C/T | 0.466721 | 0.124627 | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76453958 | ataaaaataggcaca[C/T]tgattaacttatttt | 63893 |
| rs7215770 | snp | A/T | 0.0785177 | 0.181917 | intron-variant | UBE2O | GRCh38.p7 | 17:76446023 | TCCTATTAAGTGAGA[A/T]AAGTGATAGCCTCTT | 63893 |
| rs7219098 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | UBE2O | GRCh38.p7 | 17:76437652 | actcctggacccaag[C/T]gatcctccctctggc | 63893 |
| rs7219520 | snp | C/G | 0.0547245 | 0.156101 | intron-variant | UBE2O | GRCh38.p7 | 17:76447045 | CCTGCCTGCCCACTG[C/G]CACAACTTCCACCTA | 63893 |
| rs7219524 | snp | C/G | 0.479177 | 0.0998894 | intron-variant | UBE2O | GRCh38.p7 | 17:76446358 | AAAAGTGCTGGCCCC[C/G]AACAGGTTCCACTGG | 63893 |
| rs7223304 | snp | C/T | 0.497121 | 0.0378299 | intron-variant | UBE2O | GRCh38.p7 | 17:76451008 | AACGGAGCATAACTG[C/T]AAACAAAGTTAACCA | 63893 |
| rs7223553 | snp | A/G | 0.497586 | 0.0346604 | intron-variant | UBE2O | GRCh38.p7 | 17:76450810 | ATTTTTAGTAGAGAC[A/G]GGGTTTCTCCATGTT | 63893 |
| rs7223992 | snp | C/T | 0.499908 | 0.00678851 | intron-variant | UBE2O | GRCh38.p7 | 17:76429765 | ATGCCTCATGCCTGG[C/T]CTCAGCACTCCAGGA | 63893 |
| rs7225310 | snp | G/T | 0.436123 | 0.166908 | intron-variant | UBE2O | GRCh38.p7 | 17:76425307 | CTACTTGGCTCATAT[G/T]GTATTTTTTTAAATA | 63893 |
| rs7503549 | snp | A/G | 0 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76406818 | AATTCTCCCGTCTCA[A/G]CCTCCCGAGTAGGTG | 63893 |
| rs8066058 | snp | A/T | 0.0547245 | 0.156101 | intron-variant | UBE2O | GRCh38.p7 | 17:76413909 | AATGGGGCCTCCTGT[A/T]GGAGCTGGACTCCTC | 63893 |
| rs8071034 | snp | A/G/T | 0.0437457 | 0.141368 | intron-variant | UBE2O | GRCh38.p7 | 17:76415927 | cacatgcacatacac[A/G/T]tatatacgtatgcgt | 63893 |
| rs8072743 | snp | A/G | 0.171057 | 0.237209 | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76454472 | cctgggcaacagagc[A/G]agactctgtctcaaa | 63893 |
| rs8076732 | snp | C/T | 0.0788843 | 0.182262 | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76454542 | CTCTAGggccaggcg[C/T]ggtggctcatgcctg | 63893 |
| rs8076798 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | UBE2O | GRCh38.p7 | 17:76416056 | gtgtacatatgtaca[C/T]acacgtatatacgta | 63893 |
| rs8076935 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | UBE2O | GRCh38.p7 | 17:76416094 | acatatgtaCAtaca[C/T]gtatatgcgtatgtg | 63893 |
| rs9894536 | snp | A/G | 0.317692 | 0.240661 | intron-variant | UBE2O | GRCh38.p7 | 17:76421657 | GGCGTGAGCCACCAC[A/G]CCCGGCCCTGAGTGA | 63893 |
| rs9895309 | snp | A/G | 0.49306 | 0.0584955 | intron-variant | UBE2O | GRCh38.p7 | 17:76438892 | GACGCCATGCACACC[A/G]AGGGCACAGAGGACA | 63893 |
| rs9896887 | snp | A/G | 0.409041 | 0.192888 | intron-variant | UBE2O | GRCh38.p7 | 17:76447977 | GCAGGATCATATCGG[A/G]GTTAGGAAGATAGAC | 63893 |
| rs9903640 | snp | C/G | 0.426201 | 0.177351 | intron-variant | UBE2O | GRCh38.p7 | 17:76432921 | ATGGCTATAAACAAA[C/G]TGACAGTCACAAGCA | 63893 |
| rs9908579 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76415797 | caacagagcaagact[C/G]tgtgtgtgtgtgtgt | 63893 |
| rs9910471 | snp | C/G | 0.431177 | 0.172264 | intron-variant | UBE2O | GRCh38.p7 | 17:76397397 | AGCCCTTCTGCTCAG[C/G]ACCCAGCAGGTGGGG | 63893 |
| rs9913840 | snp | G/T | 0.461148 | 0.133852 | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76451779 | TGTGAGATACAGGGG[G/T]GTGTGTGTGTGTGTG | 63893 |
| rs9914927 | snp | C/T | 0.428635 | 0.174898 | intron-variant | UBE2O | GRCh38.p7 | 17:76413041 | CAAAACAAAATGAAA[C/T]AAAAAAACCCAACTC | 63893 |
| rs10647924 | in-del | -/TT/TTT/TTTT | 0.093417 | 0.194889 | intron-variant | UBE2O | GRCh38.p7 | 17:76419123 | AGATTTTTTTTTTTT[-/TT/TTT/TTTT]AAATTAGGCCTGGTG | 63893 |
| rs10852769 | snp | C/T | 0.477853 | 0.102875 | intron-variant | UBE2O | GRCh38.p7 | 17:76419939 | ATTCCTCGGCCATGG[C/T]CCTCGGGACCCTGGT | 63893 |
| rs11077815 | snp | C/T | 0.496382 | 0.0423778 | intron-variant | UBE2O | GRCh38.p7 | 17:76393809 | GTGTGGGATCTCAAC[C/T]GACAGGGCAATGGGC | 63893 |
| rs11077816 | snp | C/T | 0.426047 | 0.177503 | intron-variant | UBE2O | GRCh38.p7 | 17:76424960 | actgcaagctccgcc[C/T]cccaggttcatgcca | 63893 |
| rs11077817 | snp | C/T | 0.498927 | 0.0231381 | intron-variant | UBE2O | GRCh38.p7 | 17:76446331 | GTTATACACGACAAT[C/T]GCACCCTTTTAAAAA | 63893 |
| rs11275244 | in-del | -/AGGAAAGA | 0.5 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76417707 | GCCTTCGACTACAGG[-/AGGAAAGA]ATGCTAAGCATGTCC | 63893 |
| rs11325407 | in-del | -/A | 0.22339 | 0.24858 | intron-variant | UBE2O | GRCh38.p7 | 17:76446463 | AAAACAAAAACAAAC[-/A]AAAAAAAAAACCAAA | 63893 |
| rs11329304 | in-del | -/C | 0 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76410769 | TGCCAGGAGCACTCT[-/C]CCTCCACGGCTGCCT | 63893 |
| rs11361245 | in-del | -/A | 0.5 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76442096 | AGGCGGGGTTCTTAC[-/A]GGGGAAATGCAGCCA | 63893 |
| rs11539331 | snp | A/T | | | missense | UBE2O | GRCh38.p7 | 17:76401024 | AGAGCAAGTTCCGAG[A/T]GGTGGTGGAAGAGGT | 63893 |
| rs11650513 | snp | A/T | 0.434976 | 0.168179 | intron-variant | UBE2O | GRCh38.p7 | 17:76443114 | CAGGAGGAAATATAT[A/T]TACATAAGCATACAG | 63893 |
| rs11652750 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76412611 | AGCTTGAAGGGTCTA[A/G]CTCCACGCTGCCATG | 63893 |
| rs11652985 | snp | C/G | 0.380529 | 0.213219 | intron-variant | UBE2O | GRCh38.p7 | 17:76402433 | ACAGAAATAGGCCAC[C/G]GCAGATAAGGAGAAC | 63893 |
| rs11653690 | snp | A/C | 0.485187 | 0.0847778 | intron-variant | UBE2O | GRCh38.p7 | 17:76446464 | AAACAAAAACAAACA[A/C]AAAAAAAAACCAAAC | 63893 |
| rs11657501 | snp | A/G | 0.439641 | 0.162899 | intron-variant | UBE2O | GRCh38.p7 | 17:76448969 | GAAAGGAAGAAGCAT[A/G]TAAGAGACACTGGCC | 63893 |
| rs11658225 | snp | A/C | 0.180914 | 0.240265 | intron-variant | UBE2O | GRCh38.p7 | 17:76446462 | AAAAACAAAAACAAA[A/C]AAAAAAAAAAACCAA | 63893 |
| rs11871786 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76441299 | TACCATATTTACATC[C/T]TAAAATGAAATGAAA | 63893 |
| rs12165049 | snp | C/T | 0.180702 | 0.240204 | intron-variant | UBE2O | GRCh38.p7 | 17:76435383 | TATTTGCATATATTA[C/T]CTGTTTAAATATACA | 63893 |
| rs12449452 | snp | C/G | 0.473726 | 0.111565 | intron-variant | UBE2O | GRCh38.p7 | 17:76447182 | TGATTCATGTTGGAT[C/G]AGGGCACTCGGTCAC | 63893 |
| rs12449930 | snp | C/T | 0.379942 | 0.213577 | intron-variant | UBE2O | GRCh38.p7 | 17:76423251 | GGGCACGGTGGTACG[C/T]ACCTGGAGCCCCAGC | 63893 |
| rs12451274 | snp | A/T | 0.499996 | 0.00139776 | intron-variant | UBE2O | GRCh38.p7 | 17:76440568 | cctggcctcaagtga[A/T]ccgcctggcttggcc | 63893 |
| rs12452388 | snp | A/G | 0 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76392143 | AGGGAGGGAGGCCAA[A/G]GTTGGCAGGGGTGGA | 63893 |
| rs12453011 | snp | C/T | 0.477768 | 0.103061 | intron-variant | UBE2O | GRCh38.p7 | 17:76418218 | TGTTTTCTATACTAT[C/T]AGGCAAAAAACTTCC | 63893 |
| rs12453375 | snp | A/G | 0.317692 | 0.240661 | intron-variant | UBE2O | GRCh38.p7 | 17:76446568 | AAAGCAAAAACACAC[A/G]GAAACTGAAGGGAAC | 63893 |
| rs12601703 | snp | C/T | 0.0894459 | 0.191631 | intron-variant | UBE2O | GRCh38.p7 | 17:76445234 | CTTTTTTTTTTTCTT[C/T]TTCCAAGCATGACTC | 63893 |
| rs12602544 | snp | A/G | 0.0221141 | 0.102801 | intron-variant | UBE2O | GRCh38.p7 | 17:76438819 | TTTGTTCACACTTCC[A/G]GGTCATTTTGTGTGA | 63893 |
| rs12935915 | snp | G/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76411052 | GGGGGAGGGGGTGGG[G/T]GGGAAGAacagagtt | 63893 |
| rs12936809 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76429522 | actccagcctgggtg[A/G]cagagtgagactctg | 63893 |
| rs12936820 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76429532 | gggtgacagagtgag[A/C]ctctgtctcaaaaaa | 63893 |
| rs12936826 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76429542 | gtgagactctgtctc[A/C]aaaaaaaaaaaaaaa | 63893 |
| rs12941950 | snp | G/T | 0.114738 | 0.210248 | intron-variant | UBE2O | GRCh38.p7 | 17:76420311 | CCCCGGGGGCCAAGT[G/T]CCCACTGAAGTGGGA | 63893 |
| rs12942557 | snp | G/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76450616 | GGTGCCTCAAAGTTG[G/T]TGttttttttttctt | 63893 |
| rs12942565 | snp | G/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76450617 | GTGCCTCAAAGTTGT[G/T]Gttttttttttcttt | 63893 |
| rs12949638 | snp | C/T | 0.0998734 | 0.199905 | intron-variant | UBE2O | GRCh38.p7 | 17:76448676 | TAAACGCTTTGCCTC[C/T]GAAACGAAGGCTGAA | 63893 |
| rs12950218 | snp | A/G | 0.100231 | 0.200173 | intron-variant | UBE2O | GRCh38.p7 | 17:76413465 | aaaaaaaacctgagt[A/G]cattaatatacatgt | 63893 |
| rs16968960 | snp | A/G | 0.434687 | 0.168495 | intron-variant | UBE2O | GRCh38.p7 | 17:76446860 | GAGGTTGCTTCATTC[A/G]ACATTGAGGGGCAGT | 63893 |
| rs17596582 | snp | A/T | 0.0998734 | 0.199905 | intron-variant | UBE2O | GRCh38.p7 | 17:76442038 | TGCTGATAACCATTC[A/T]GGAAACCCACGTGTG | 63893 |
| rs28452498 | snp | C/G | 0.345925 | 0.230864 | intron-variant | UBE2O | GRCh38.p7 | 17:76421371 | TGACTATTTTCTTTT[C/G]TCTTTTTTTTTTTGA | 63893 |
| rs28507667 | snp | A/C | 0.0360663 | 0.129354 | intron-variant | UBE2O | GRCh38.p7 | 17:76437519 | AGTATCCTGGATTGG[A/C]TCCTGGAAAAGAAAA | 63893 |
| rs28615986 | snp | C/G | 0.181022 | 0.240296 | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76455188 | CCCAACACTTTGACT[C/G]CGCCTGAAATCCCAA | 63893 |
| rs28709924 | snp | C/G | 0.179744 | 0.239925 | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76452313 | CTCCCTGCACGGACC[C/G]GGCACGGCCTTCATT | 63893 |
| rs28715905 | snp | A/C | 0.171057 | 0.237209 | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76451981 | TCAGGTCAAGAAAAA[A/C]CCTTCGGGTTTCCAA | 63893 |
| rs33950096 | in-del | -/A | | | downstream-variant-500B | UBE2O | GRCh38.p7 | 17:76389511 | TGCTAATGAGCCAAC[-/A]AAAAAAAAAAAAAAA | 63893 |
| rs33997542 | in-del | -/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76418587 | TTTTTTTTTTTTTTT[-/T]GAGACGGAGTCTCGC | 63893 |
| rs34045939 | in-del | -/GT | | | intron-variant | UBE2O | GRCh38.p7 | 17:76415805 | AAGACTGTGTGTGTG[-/GT]TGTGTGTGTGTGTGT | 63893 |
| rs34070229 | snp | C/T | 0.0203244 | 0.0987377 | missense | UBE2O | GRCh38.p7 | 17:76391374 | CCTTCTCCAGCAGGG[C/T]ATGGGTTTCCAGCCA | 63893 |
| rs34110427 | in-del | -/G | | | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76451779 | GTGAGATACAGGGGT[-/G]GTGTGTGTGTGTGTG | 63893 |
| rs34127040 | in-del | -/TCTGTG/TG | | | intron-variant | UBE2O | GRCh38.p7 | 17:76415795 | GCAACAGAGCAAGAC[-/TCTGTG/TG]TGTGTGTGTGTGTGT | 63893 |
| rs34131823 | in-del | -/G | | | frameshift-variant | UBE2O | GRCh38.p7 | 17:76391306 | AGCTCGGCTACAGCT[-/G]GGGGGCTCTGGCGAG | 63893 |
| rs34139956 | in-del | -/A | | | intron-variant | UBE2O | GRCh38.p7 | 17:76440700 | CAGAGCAGAGGTGGG[-/A]AAACTACAGCCTGCA | 63893 |
| rs34234366 | snp | A/C | 0.100231 | 0.200173 | intron-variant | UBE2O | GRCh38.p7 | 17:76402429 | AGCAACAGAATTAGG[A/C]CACGGCAGATAAGGA | 63893 |
| rs34281174 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76414456 | TGGGGAGACCAGAAA[C/G]TGAGTCCTGTCTGGA | 63893 |
| rs34359853 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76403288 | TTATTATTTTTTTTA[C/G]AGACAGGGTCTTGCT | 63893 |
| rs34371138 | snp | A/C/G | 8.23961e-05 | 0.00641804 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76396276 | GGGCTTGTCCTCCTT[A/C/G]CGCTCTACGTCGGGC | 63893 |
| rs34471769 | snp | C/T | 0.0106691 | 0.0722546 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76399652 | TGCGTCCTGCTCTGC[C/T]GAGTGCAGCCTGTCA | 63893 |
| rs34581713 | in-del | -/A | | | intron-variant | UBE2O | GRCh38.p7 | 17:76443281 | CAAAAAAAGTTGGGG[-/A]AATATATATATATTT | 63893 |
| rs34603906 | snp | C/T | 3.2956e-05 | 0.00405918 | missense | UBE2O | GRCh38.p7 | 17:76399714 | GCTGCTCTCCTGCCT[C/T]GTGGGGCTCCTCTGC | 63893 |
| rs34663450 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76392810 | ATACAAAAATTAGCC[A/G]GGCGTGGTGATGCAT | 63893 |
| rs34701429 | in-del | -/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76397253 | ATATCCTGCTGCGTT[-/C]CCCTGGAATGGCCGT | 63893 |
| rs34970361 | in-del | -/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76403407 | TGAGTAGCTGGGACT[-/C]ACAGGCATGCATCAC | 63893 |
| rs35062714 | in-del | -/A | | | intron-variant | UBE2O | GRCh38.p7 | 17:76419308 | AAAAAAAAAAAAAAA[-/A]TCCCTTTCTCCTGAA | 63893 |
| rs35177607 | snp | C/T | 0.0509478 | 0.151255 | intron-variant | UBE2O | GRCh38.p7 | 17:76393395 | CAGTCTCCTCACGCC[C/T]GGCTAATTTTTTGTA | 63893 |
| rs35252343 | snp | A/G | 0.477515 | 0.103619 | intron-variant | UBE2O | GRCh38.p7 | 17:76412578 | GCTGAGGCCTCTCTG[A/G]CTCTTTGGTTGTCCC | 63893 |
| rs35270113 | in-del | -/C | | | frameshift-variant | UBE2O | GRCh38.p7 | 17:76398318 | ACGATGTCAGTTGTA[-/C]CGGAACCTAAAGTCA | 63893 |
| rs35319167 | snp | A/G | 0.213635 | 0.247341 | intron-variant | UBE2O | GRCh38.p7 | 17:76448280 | CTATCTGAATAAAAC[A/G]CAATTTAGATTCACT | 63893 |
| rs35352400 | in-del | -/AG/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76442096 | GGCGGGGTTCTTACA[-/AG/G]GGGGAAATGCAGCCA | 63893 |
| rs35392031 | in-del | -/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76444182 | CCAAGGTTGCACCAC[-/G]TGCACTCCAGCCTGG | 63893 |
| rs35450208 | in-del | -/A | | | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76455127 | GTGAGATTCCGTCTC[-/A]AAAAAAAGTAACTCT | 63893 |
| rs35480209 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76392786 | GGTGAAACCCCGTCT[C/G]TACTAAAAATACAAA | 63893 |
| rs35551260 | in-del | -/AT/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76443282 | AAAAAAAGTTGGGGA[-/AT/T]ATATATATATATTTT | 63893 |
| rs35593511 | in-del | -/G | | | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76452041 | GATTATTTTTTTCAA[-/G]GGAGTCCATATGCAC | 63893 |
| rs35597500 | in-del | -/T | | | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76451778 | TGTGAGATACAGGGG[-/T]GGTGTGTGTGTGTGT | 63893 |
| rs35739452 | in-del | -/A | | | intron-variant | UBE2O | GRCh38.p7 | 17:76406618 | CTCACAAAAAAAAAA[-/A]GGAAAGAAAAGCAAT | 63893 |
| rs35867938 | in-del | -/A/AA | | | intron-variant | UBE2O | GRCh38.p7 | 17:76437149 | TGAGACTCCATCTTT[-/A/AA]AAAAAAAAAAAAAAA | 63893 |
| rs35899458 | in-del | -/A | | | intron-variant | UBE2O | GRCh38.p7 | 17:76399968 | GAGGTGCACCTGGGC[-/A]AGGCCTGGCCCTAGG | 63893 |
| rs35928801 | snp | G/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76392807 | AAAATACAAAAATTA[G/T]CCAGGCGTGGTGATG | 63893 |
| rs35976162 | in-del | -/A | 0.475702 | 0.107512 | intron-variant | UBE2O | GRCh38.p7 | 17:76395055 | AATTTTTGTATTTTT[-/A]AGTAGAGACAGGGTT | 63893 |
| rs36003798 | in-del | -/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76411950 | GCCTCCCAAAGTGCT[-/G]GGGATTACAGGCGTG | 63893 |
| rs36027965 | in-del | -/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76440749 | GCCTGTTTCTTAAAA[-/T]TTTATTGGAACATGA | 63893 |
| rs36107488 | in-del | -/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76403248 | GATCTATCAGGATGA[-/C]ACTCATATATTTTAT | 63893 |
| rs55683961 | snp | A/G | 0.0807149 | 0.183963 | intron-variant | UBE2O | GRCh38.p7 | 17:76437026 | TGGTGGTGGGCACCC[A/G]TAATCCTAGCTGCTC | 63893 |
| rs55712852 | snp | A/G | | | downstream-variant-500B | UBE2O | GRCh38.p7 | 17:76389076 | AACCATTTTGGCTTA[A/G]CGTCCAGGAGTTGTG | 63893 |
| rs55829930 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | UBE2O | GRCh38.p7 | 17:76450597 | TGCAAAATCTATCCA[A/G]AGTGGTGCCTCAAAG | 63893 |
| rs56084731 | snp | A/G | 0 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76393321 | CCAGGCTGGAGTGCA[A/G]TGGTGTGATCTTGGC | 63893 |
| rs56146061 | snp | A/C | 0.47726 | 0.104176 | intron-variant | UBE2O | GRCh38.p7 | 17:76427085 | GTTTCACTGTTGAAC[A/C]TGGGGAGTAATCTGC | 63893 |
| rs56154175 | snp | C/T | 0.100231 | 0.200173 | intron-variant | UBE2O | GRCh38.p7 | 17:76423004 | AGAGATCCAGTGCCA[C/T]GGGGAAGTGTCCCTG | 63893 |
| rs56194054 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | UBE2O | GRCh38.p7 | 17:76421446 | GATCTCGGCACACCA[C/T]AGCCTGCTTCCCCGG | 63893 |
| rs56239194 | snp | C/G | 0.424814 | 0.178718 | intron-variant | UBE2O | GRCh38.p7 | 17:76407279 | TCCTTATCTCTGCTC[C/G]AAGACCCCAGGAGGC | 63893 |
| rs56248611 | snp | A/G | 0.100231 | 0.200173 | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76452173 | TGCAGCAATTAAAAG[A/G]AGGCAGCAGGGTAAA | 63893 |
| rs56276871 | snp | A/G | 0 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76393276 | TTTTTTGGCTTATGT[A/G]TTTTTTTGAGATGGA | 63893 |
| rs56280331 | snp | A/G | 0.409721 | 0.192325 | intron-variant | UBE2O | GRCh38.p7 | 17:76407157 | CCAAGGCAGCGGACC[A/G]CAGGTGGCACATGGT | 63893 |
| rs56334898 | in-del | -/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76418573 | GGAGGAACAGGTTTT[-/G]TTTTTTTTTTTTTTG | 63893 |
| rs56666001 | in-del | -/CA | | | intron-variant | UBE2O | GRCh38.p7 | 17:76435456 | ACACACACACACACA[-/CA]AAGATTAAGATTTAG | 63893 |
| rs56702273 | snp | A/G | 0.0182019 | 0.0936463 | intron-variant | UBE2O | GRCh38.p7 | 17:76436824 | TAGTGAAAGATCAAC[A/G]AGGAGCATTTATTTC | 63893 |
| rs56760827 | in-del | -/A/AAAA | 0.5 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76437165 | AAAAAAAAAAAAAAA[-/A/AAAA]GGTGGCAGGGCACAG | 63893 |
| rs56874400 | in-del | -/TG | | | intron-variant | UBE2O | GRCh38.p7 | 17:76415828 | GTGTGTGTGTGTGTG[-/TG]CATACACATATATGT | 63893 |
| rs56945001 | in-del | -/TG/TGTGTGTGTG | 0 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76415829 | GTGTGTGTGTGTGTG[-/TG/TGTGTGTGTG]CATACACATATATGT | 63893 |
| rs57167854 | in-del | -/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76446777 | TCTGCACACTTGTTT[-/T]GCTCTAGGAGGTGGA | 63893 |
| rs57586498 | in-del | -/TGCTAGTAGAAGA | 0.0119091 | 0.0762411 | intron-variant | UBE2O | GRCh38.p7 | 17:76406584 | AACTAAAACAAACTC[-/TGCTAGTAGAAGA]ACGTGACTCACAAAA | 63893 |
| rs57655728 | in-del | -/A | 0.481396 | 0.0946345 | intron-variant | UBE2O | GRCh38.p7 | 17:76431357 | AAAGATACAAAAAAA[-/A]AATTAGCTGGGCGTG | 63893 |
| rs57911746 | in-del | -/CCGAAGTACAGCGA | 0.0460142 | 0.144533 | intron-variant | UBE2O | GRCh38.p7 | 17:76426879 | CTTACTTCCTTCTTC[-/CCGAAGTACAGCGA]AGGTCTCTTAGTAAA | 63893 |
| rs57947064 | in-del | -/AAC | | | intron-variant | UBE2O | GRCh38.p7 | 17:76434815 | AACAAACAAAAAAAC[-/AAC]TTTGTCTCTGCCCTC | 63893 |
| rs58377572 | in-del | -/AAAAAAAAAAAAA | | | intron-variant | UBE2O | GRCh38.p7 | 17:76425226 | CAAGGTCCTTTCGAC[-/AAAAAAAAAAAAA]AAAAAAAAAAAAGTA | 63893 |
| rs59035745 | snp | A/G | 0.212728 | 0.247206 | intron-variant | UBE2O | GRCh38.p7 | 17:76447975 | GAGCAGGATCATATC[A/G]GGGTTAGGAAGATAG | 63893 |
| rs59151931 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76414857 | TGCACCCCTCTGTCT[G/T]GGCTCTGGGCTTGTC | 63893 |
| rs59232506 | snp | C/T | 0.0391387 | 0.134304 | intron-variant | UBE2O | GRCh38.p7 | 17:76440403 | CACGATCACGGCCCA[C/T]TGCCACCTCGACCGC | 63893 |
| rs59424179 | in-del | -/A | 0.424193 | 0.179323 | intron-variant | UBE2O | GRCh38.p7 | 17:76450082 | AAAAAAAAAAAAAAA[-/A]TCTGCCACTACATTA | 63893 |
| rs59499025 | snp | C/G | 0.0329836 | 0.124112 | intron-variant | UBE2O | GRCh38.p7 | 17:76428416 | TCTGTTTCCTGGGAG[C/G]CTTCGTCAACTTCAA | 63893 |
| rs59625228 | in-del | -/TT | 0.170408 | 0.236992 | intron-variant | UBE2O | GRCh38.p7 | 17:76433608 | TTGTCTCAATAAACC[-/TT]TTTTTTTTTAAGAGA | 63893 |
| rs59712772 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76407002 | TGCATCCAGGTATGA[A/G]CCTGTTTCAAATGAC | 63893 |
| rs59781051 | in-del | -/CACACA | | | intron-variant | UBE2O | GRCh38.p7 | 17:76435451 | ACACACACACACACA[-/CACACA]AAGATTAAGATTTAG | 63893 |
| rs59801466 | snp | C/T | 0.0821764 | 0.185298 | intron-variant | UBE2O | GRCh38.p7 | 17:76429385 | CATCTTGACAAAAAA[C/T]ACACAAATTAGCCAG | 63893 |
| rs59804987 | snp | C/T | 0.0329836 | 0.124112 | intron-variant | UBE2O | GRCh38.p7 | 17:76428058 | TGTTGTTATAGCTTA[C/T]ATAGCATTTTAAGTG | 63893 |
| rs60040913 | in-del | -/A | 0 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76393304 | GAGTATAGCTCTGTC[-/A]CCCAGGCTGGAGTGC | 63893 |
| rs60211126 | snp | C/T | 0.0391387 | 0.134304 | intron-variant | UBE2O | GRCh38.p7 | 17:76440573 | CCTCAAGTGATCCGC[C/T]TGGCTTGGCCTCCCA | 63893 |
| rs60251820 | in-del | -/TTTTCCT | 0.0349115 | 0.127424 | intron-variant | UBE2O | GRCh38.p7 | 17:76420413 | TCCTGCATCGTTTTG[-/TTTTCCT]AATACCTGTGATTTT | 63893 |
| rs60530405 | in-del | -/G | 0.0123036 | 0.0774623 | intron-variant | UBE2O | GRCh38.p7 | 17:76407952 | GAGCGACAAGGGGCT[-/G]GGGGATGGTAACATG | 63893 |
| rs60762375 | snp | C/T | 0.0448719 | 0.142907 | intron-variant | UBE2O | GRCh38.p7 | 17:76428111 | CTTTAGCTCAAGCTA[C/T]CATGTCACTGAAACA | 63893 |
| rs60950120 | in-del | -/TACACACACACACA | | | intron-variant | UBE2O | GRCh38.p7 | 17:76435417 | ACACACACACACACA[-/TACACACACACACA]CACACACACACACAC | 63893 |
| rs61016259 | in-del | -/A/AAAAAA | 0.5 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76425250 | AAAAAAAAAAAAAAA[-/A/AAAAAA]GTAAAAGAAAAAAAT | 63893 |
| rs61028962 | snp | C/T | 0.206642 | 0.246211 | intron-variant | UBE2O | GRCh38.p7 | 17:76407913 | CATTTCTCCAAAGAC[C/T]TGATGGTGCTGGGAG | 63893 |
| rs61081315 | in-del | -/A | | | intron-variant | UBE2O | GRCh38.p7 | 17:76429564 | AAAAAAAAAAAAAAA[-/A]GTTAAAAAAGTTGAG | 63893 |
| rs61194660 | snp | C/G | 0.0948562 | 0.196037 | intron-variant | UBE2O | GRCh38.p7 | 17:76392300 | TCTCTCTCTGCAGAA[C/G]AGCCTGGAATCTTTT | 63893 |
| rs61271197 | snp | C/T | 0.0547245 | 0.156101 | intron-variant | UBE2O | GRCh38.p7 | 17:76439897 | GGAACTAGGCTCTCG[C/T]TCCCTTATGTGCATC | 63893 |
| rs61392902 | snp | G/T | 0.0228947 | 0.104514 | intron-variant | UBE2O | GRCh38.p7 | 17:76433665 | GAGGTGGAGTGAGTA[G/T]TGCGCCACTGCATTC | 63893 |
| rs61601720 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76392764 | TCAAGAGCAGTCTGG[C/G]CAACGTGGTGAAACC | 63893 |
| rs61619670 | snp | C/T | 0.0463947 | 0.145069 | intron-variant | UBE2O | GRCh38.p7 | 17:76446595 | GAACAGAAACTGAAA[C/T]TGAGGTGGAACTCAG | 63893 |
| rs61758457 | snp | G/T | | | synonymous-codon | UBE2O | GRCh38.p7 | 17:76399709 | GGGCAGCTGCTCTCC[G/T]GCCTCGTGGGGCTCC | 63893 |
| rs62084962 | snp | C/T | 0.498813 | 0.0243321 | intron-variant | UBE2O | GRCh38.p7 | 17:76392900 | GAGGTTGCAGTGAGC[C/T]GAGATTGTGCCATTG | 63893 |
| rs62084964 | snp | A/G/T | 4.74327e-05 | 0.00486971 | intron-variant | UBE2O | GRCh38.p7 | 17:76400573 | TGGCAGGTGGGACAC[A/G/T]CCAGTCAGGGCAGGC | 63893 |
| rs62084966 | snp | C/T | 0.5 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76418910 | TCAGCTTGAAAAACA[C/T]GGATTTTTCAACCCA | 63893 |
| rs62084967 | snp | A/G | 0.173643 | 0.238054 | intron-variant | UBE2O | GRCh38.p7 | 17:76424012 | TCCCAAGTTCACGCC[A/G]TTCTCCTGCCTCAGC | 63893 |
| rs62084968 | snp | A/C | 0.00557542 | 0.0525036 | intron-variant | UBE2O | GRCh38.p7 | 17:76426302 | CACCATGCCCAGCCA[A/C]AAGAACTTTTTTCTA | 63893 |
| rs62084970 | snp | C/G | 0.47743 | 0.103805 | intron-variant | UBE2O | GRCh38.p7 | 17:76429021 | ATTCTCCTGCCTCAG[C/G]CTCCCGAGTAGCTGG | 63893 |
| rs62084971 | snp | G/T | 0.173643 | 0.238054 | intron-variant | UBE2O | GRCh38.p7 | 17:76429236 | CTTCCTATGCATCTA[G/T]AATTATTTCAAAATA | 63893 |
| rs62084972 | snp | C/G | 0.381113 | 0.21286 | intron-variant | UBE2O | GRCh38.p7 | 17:76429316 | TGAGGCTGAGGTGGG[C/G]AGATCACTTGAGCTC | 63893 |
| rs62085016 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76445418 | AAATGCAAACCAACT[A/C]AAAATCCCCCAACCA | 63893 |
| rs66523654 | in-del | -/TTT | 0.375 | 0.216506 | cds-indel | UBE2O | GRCh38.p7 | 17:76389850 | TGCTTTTGAGTTTTT[-/TTT]CCAACCTTAAATATT | 63893 |
| rs66597649 | snp | C/T | 0.471292 | 0.116318 | intron-variant | UBE2O | GRCh38.p7 | 17:76403803 | ACAAAAAGTACAAGA[C/T]GAGCCTGGCACATCT | 63893 |
| rs66640416 | in-del | -/TA | 0 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76435417 | ACACACACACACACA[-/TA]CACACACACACACAC | 63893 |
| rs66686654 | snp | A/T | 0.100588 | 0.200439 | intron-variant | UBE2O | GRCh38.p7 | 17:76434228 | TAGACCTAGACATAC[A/T]TGGAAACCCAGCACA | 63893 |
| rs66834782 | in-del | -/TT | 0 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76406704 | TTTTTTTTTTTTTTT[-/TT]GAGATGGAGTCTCGC | 63893 |
| rs67549832 | in-del | -/ACTA/CTAA | 0.5 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76431653 | TAGGGAAAAGAAAGA[-/ACTA/CTAA]CTATTAGGGCCAGAC | 63893 |
| rs67873924 | snp | C/G | 0.100588 | 0.200439 | intron-variant | UBE2O | GRCh38.p7 | 17:76433910 | GGCGGTGCGCGCCTA[C/G]AGGCCCAGCTACAGT | 63893 |
| rs67911712 | in-del | -/AAA | 0.5 | 0 | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76454328 | GAAAAAAAAAAAAAA[-/AAA]TAGCTGGGCGTGGTG | 63893 |
| rs71280850 | in-del | -/AC | 0.5 | 0 | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76451803 | TCCTATCAGTAATTG[-/AC]ACACACACACACACA | 63893 |
| rs71280851 | in-del | -/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76401874 | AGAAAGTATTAGAAC[-/T]TTTTTTTTTTTTTTT | 63893 |
| rs71325784 | multinucleotide-polymorphism | ATTA/TCAG | 0 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76423543 | CTAAAAATACAAAAA[ATTA/TCAG]GCCAGGCATGGTGGC | 63893 |
| rs71363634 | in-del | -/G | 0.5 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76431370 | TACAAAAAAAAATTA[-/G]CTGGGCGTGCTGGTG | 63893 |
| rs71384104 | snp | A/C | 0.5 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76408801 | TGTGAACAAAACTAA[A/C]CCTTGGAATAAACCC | 63893 |
| rs71384105 | snp | G/T | 0.444444 | 0.157135 | intron-variant | UBE2O | GRCh38.p7 | 17:76443600 | AGTCAGAACATTTTT[G/T]TTTTTTTTAAGTCCA | 63893 |
| rs72007909 | in-del | -/A | | | intron-variant | UBE2O | GRCh38.p7 | 17:76425226 | AAGGTCCTTTCGACA[-/A]AAAAAAAAAAAAAAA | 63893 |
| rs72858197 | snp | C/T | 0.416382 | 0.186593 | intron-variant | UBE2O | GRCh38.p7 | 17:76409259 | AGGCGTGAGCCACCG[C/T]GCCCAGCCTATTGTC | 63893 |
| rs72858198 | snp | C/T | 0.288386 | 0.247035 | intron-variant | UBE2O | GRCh38.p7 | 17:76416138 | ATATATGTGCGTGTA[C/T]AGATATATAAAGTGT | 63893 |
| rs72858200 | snp | C/G | 0.0236746 | 0.106192 | intron-variant | UBE2O | GRCh38.p7 | 17:76416314 | ATCTTCCCTGAGCTT[C/G]CTGGAAACGCAGACT | 63893 |
| rs72860804 | snp | A/G | 0.100231 | 0.200173 | intron-variant | UBE2O | GRCh38.p7 | 17:76417821 | GATGCATCAGCGTCC[A/G]CGAAGAGACGTCTGG | 63893 |
| rs72860817 | snp | A/T | 0.0414363 | 0.137845 | intron-variant | UBE2O | GRCh38.p7 | 17:76443057 | GGTGAAGTGCTATCA[A/T]GTCTGCCACTAACTT | 63893 |
| rs73357578 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE2O | GRCh38.p7 | 17:76396879 | CACCTCCCCACCACT[A/G]AGGAGGAGCTCTGGG | 63893 |
| rs73357595 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | UBE2O | GRCh38.p7 | 17:76410557 | GAGAAGGTGGGTCTG[C/T]GGACCAGCCTCTGGA | 63893 |
| rs73359803 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | UBE2O | GRCh38.p7 | 17:76419037 | GCTGTAATACCAGTA[C/T]TTTGAGAGGCTGAGC | 63893 |
| rs73359804 | snp | A/C | 0.00279162 | 0.0372561 | intron-variant | UBE2O | GRCh38.p7 | 17:76419528 | TTCGGCACTCCCTGA[A/C]ACACCCTTCCTGTGG | 63893 |
| rs73359807 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | UBE2O | GRCh38.p7 | 17:76419723 | CCCGCCAGCACGCAT[C/T]CTTGGGAACCTGGTG | 63893 |
| rs73363345 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | UBE2O | GRCh38.p7 | 17:76428848 | TTGTCTGTGATTATA[C/T]AAGACATGACCATCA | 63893 |
| rs73363350 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | UBE2O | GRCh38.p7 | 17:76430731 | GTTTCACAATCCTCA[A/G]CATGTTAACTGAAGG | 63893 |
| rs73363363 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant | UBE2O | GRCh38.p7 | 17:76445804 | TTCCCTGGCTATAAC[C/T]GCACACATCAAGTGG | 63893 |
| rs73363369 | snp | A/G | 0.00835141 | 0.0640778 | utr-variant-5-prime, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76453459 | CCGAGGAAGAGGGGA[A/G]TGGTCGGGGTGGGGC | 63893 |
| rs73996364 | snp | C/T | 0.0603597 | 0.1629 | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390374 | GTGGTCGACAGGCCA[C/T]GTATAGCCGGGAGTC | 63893 |
| rs73996365 | snp | C/G | 0.0543475 | 0.155628 | intron-variant | UBE2O | GRCh38.p7 | 17:76397640 | GCCAACTGCAGGCCT[C/G]CACCAAGGGCTGTGT | 63893 |
| rs73996375 | snp | C/T | 0.0547245 | 0.156101 | intron-variant | UBE2O | GRCh38.p7 | 17:76426462 | TGGATTTATTTCTAC[C/T]ACCTTTAGGGCTTTC | 63893 |
| rs73996379 | snp | A/G | 0.0543475 | 0.155628 | intron-variant | UBE2O | GRCh38.p7 | 17:76435702 | CAATCACAGGTCTAC[A/G]TGCCCTCTCTAAGCC | 63893 |
| rs73996382 | snp | A/G | 0.0547245 | 0.156101 | intron-variant | UBE2O | GRCh38.p7 | 17:76438792 | TCTTCCACTGAATAC[A/G]GAATGAAGATGTTTG | 63893 |
| rs74177007 | snp | A/C | 0 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76423520 | AACATGGTGAAACCC[A/C]GTCTCTACTAAAAAT | 63893 |
| rs74177008 | snp | A/T | 0 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76423534 | CAGTCTCTACTAAAA[A/T]TACAAAAAATTAGCC | 63893 |
| rs74177009 | snp | A/T | 0 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76423562 | GCCAGGCATGGTGGC[A/T]CGTACCTATAGTCCC | 63893 |
| rs74177010 | snp | A/G | 0 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76423603 | GGGGCTGAGGCAGGA[A/G]AATCGCTTGAACCTG | 63893 |
| rs74189806 | snp | C/G | 0 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76423629 | ACCTGGGAGGCGGAG[C/G]TTGCAGTGAGCCGAG | 63893 |
| rs74189916 | snp | C/T | 0 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76423624 | CTTGAACCTGGGAGG[C/T]GGAGCTTGCAGTGAG | 63893 |
| rs74194575 | multinucleotide-polymorphism | AC/GA | 0 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76423620 | ATCGCTTGAACCTGG[AC/GA]GGCGGAGCTTGCAGT | 63893 |
| rs74194889 | in-del | -/CATACGTATATACGTGTATGTGCATATGTATACG | 0 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76415974 | GTACATATGTATACA[lengthTooLong]CATACGTATATACGT | 63893 |
| rs74368909 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | UBE2O | GRCh38.p7 | 17:76414061 | GAGCCCTGATAACCC[A/G]GCAATCAGCTCACTG | 63893 |
| rs74388821 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | UBE2O | GRCh38.p7 | 17:76410429 | CTGAGCATCTAACAA[C/T]GCACAGGACATCCCT | 63893 |
| rs74405259 | snp | G/T | 0.5 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76451232 | AGACACCAGCAATCA[G/T]CTGGTGTCACACAGT | 63893 |
| rs74513803 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76414612 | GTGCTGCTGCATCAC[C/T]GCCTGGAAACTCGGC | 63893 |
| rs74521038 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76440086 | GACAGTAAACAGGAC[A/G]TGAAGTAGTATAATC | 63893 |
| rs74588673 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBE2O | GRCh38.p7 | 17:76445738 | GAGTTATCCAGTAAC[A/G]CAATTCAATTTTATT | 63893 |
| rs74721266 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | UBE2O | GRCh38.p7 | 17:76427206 | TCTCTTTTATCTCTG[C/T]AGAATTCTAACTAAC | 63893 |
| rs74766765 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBE2O | GRCh38.p7 | 17:76430804 | GCAAAGAAGCTGCAA[C/T]ATCTTTTGGCCCTTT | 63893 |
| rs74797237 | snp | G/T | 0.040671 | 0.13668 | intron-variant | UBE2O | GRCh38.p7 | 17:76445984 | TGGAGCCTCAGGAAG[G/T]AGCTACAGTTAAAAA | 63893 |
| rs74839097 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76450525 | CAATGACAAAATACC[A/C]CCACCGAGCCACAAA | 63893 |
| rs74878702 | snp | C/T | 0.0981749 | 0.200216 | intron-variant | UBE2O | GRCh38.p7 | 17:76438639 | TTCTCTTAGGTTCGA[C/T]AGATTTCAGATTTTA | 63893 |
| rs74941845 | in-del | -/T/TAAA | | | intron-variant | UBE2O | GRCh38.p7 | 17:76423728 | AAATAAATAAATAAA[-/T/TAAA]AAATAAGGTCAGGCA | 63893 |
| rs74984887 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | UBE2O | GRCh38.p7 | 17:76420629 | TAACTACATCTTTGC[A/G]AGACAAACTGGGCTG | 63893 |
| rs75020011 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | UBE2O | GRCh38.p7 | 17:76438512 | AACACATGCTTTACC[A/T]GTTATTCCTCAAACG | 63893 |
| rs75022324 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | UBE2O | GRCh38.p7 | 17:76430572 | ATCAGATCCTCGATG[C/T]AGATGATGCCATATT | 63893 |
| rs75094980 | snp | A/C | 0.5 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76437449 | AGCGAGATTCCATCT[A/C]AAAAAAAAAAAAAAA | 63893 |
| rs75159023 | snp | A/G | 6.59239e-05 | 0.00574087 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76396267 | CTGCCCCTCGGGCTT[A/G]TCCTCCTTGCGCTCT | 63893 |
| rs75168214 | snp | A/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76419136 | AGATTTTTTTTTTTT[A/T]AATTAGGCCTGGTGG | 63893 |
| rs75308795 | snp | A/C | 0.0456336 | 0.143994 | intron-variant | UBE2O | GRCh38.p7 | 17:76447757 | TTCCTATGCCCCTGA[A/C]ACAACCACCTTCCCC | 63893 |
| rs75324038 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | UBE2O | GRCh38.p7 | 17:76435276 | TCACACACATAGAGT[C/T]TGGTCACAGTGGCTA | 63893 |
| rs75444317 | snp | C/G | | | stop-gained | UBE2O | GRCh38.p7 | 17:76401066 | ACGGGCTTGACACCT[C/G]ACAGCCACTGGACGC | 63893 |
| rs75721035 | snp | C/T | 0.0399052 | 0.1355 | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76451606 | CGTTCCTCTGTAGTC[C/T]TTGTCTCCCACTGTG | 63893 |
| rs75770006 | snp | A/G | 0.5 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76392962 | CTCAAAAAAAAAAAA[A/G]GATTGTATTCCTCAG | 63893 |
| rs75776105 | snp | C/T | 0.5 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76444711 | GACATCCATTTCCCC[C/T]AGTACAGTGCTGGGA | 63893 |
| rs75803763 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76404922 | TTTCCAATAATTTAT[C/T]TTTTTAAAGAAATGT | 63893 |
| rs75812062 | snp | C/T | 0.5 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76392311 | AGAACAGCCTGGAAT[C/T]TTTTTTTTTTGAGAC | 63893 |
| rs75833979 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76416677 | TACCATCCCGGGATG[C/G]TGGCATCACTGGGAC | 63893 |
| rs76110889 | snp | A/G | 0.0137897 | 0.0818821 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76396168 | GACCTCGCCCTTGGC[A/G]CTGGTGAAGGTGACG | 63893 |
| rs76160849 | snp | A/G | 0.0729998 | 0.176553 | intron-variant | UBE2O | GRCh38.p7 | 17:76428211 | TTTTGTATGTGACCC[A/G]TTTTTGCTCTTCGGA | 63893 |
| rs76162859 | snp | A/G | 0.0441095 | 0.141807 | intron-variant | UBE2O | GRCh38.p7 | 17:76425543 | TTATAGACATTATCT[A/G]TTGACGTCCTGTTTT | 63893 |
| rs76196968 | snp | A/G | 0.5 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76392963 | TCAAAAAAAAAAAAA[A/G]ATTGTATTCCTCAGC | 63893 |
| rs76308755 | snp | C/T | 0.0178098 | 0.0926698 | intron-variant | UBE2O | GRCh38.p7 | 17:76417526 | CCACCTCCTTGTTAA[C/T]ATGGTCAAAATTCTC | 63893 |
| rs76382452 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76410386 | GGGTGGTGGGGGTTC[C/T]GGTATCTAGTGGGCA | 63893 |
| rs76391088 | snp | G/T | 0.5 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76428920 | TTTTTTTTTTTTTTT[G/T]AGATGGAGTCTTGCT | 63893 |
| rs76490095 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76405822 | CACCAGAGGCACTTG[A/G]CTTGCCGGAGGTAGC | 63893 |
| rs76520700 | snp | A/T | 0.5 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76424864 | CTTTTTTTTTTTTTA[A/T]TTTTTATTTTTTTTT | 63893 |
| rs76650746 | in-del | -/ATAAA | | | intron-variant | UBE2O | GRCh38.p7 | 17:76423716 | AAATAAATAAATAAA[-/ATAAA]TAAATAAATAAAAAA | 63893 |
| rs76668050 | snp | A/G | 0.00438332 | 0.0466095 | intron-variant | UBE2O | GRCh38.p7 | 17:76442369 | CAACACACCTAGTAC[A/G]GGGGGTGGGAGACAG | 63893 |
| rs76758803 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76438986 | ACCTTGTAAACTGCC[A/G]CCAAATCACCCATTG | 63893 |
| rs76870210 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76438381 | AAGAAAAACTTAAAG[A/G]CTCCTCGTCGCTCTT | 63893 |
| rs76891045 | snp | C/G | 0.00636936 | 0.0560724 | intron-variant | UBE2O | GRCh38.p7 | 17:76442010 | TAGCCATCCTCCTAA[C/G]GTGAGGACTGGGTGC | 63893 |
| rs77042512 | snp | C/G | 0.00874735 | 0.0655527 | intron-variant | UBE2O | GRCh38.p7 | 17:76448186 | AGGGCACTGAGGCCC[C/G]AGGGCTAGAAGGGGA | 63893 |
| rs77143592 | snp | C/G | 0.0425829 | 0.139564 | intron-variant | UBE2O | GRCh38.p7 | 17:76412392 | GCCACTCCTCCACCC[C/G]CTCCCTGACCCCCCA | 63893 |
| rs77352655 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76446465 | AACAAAAACAAACAA[A/C]AAAAAAAACCAAACA | 63893 |
| rs77500959 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76404522 | CAACTCAATGCAAGA[C/T]GTGTTCCTGAATTGG | 63893 |
| rs77535221 | snp | A/C | 0.0901694 | 0.192235 | intron-variant | UBE2O | GRCh38.p7 | 17:76395513 | GTAATTTTTTAAAGG[A/C]GGGAGGAAAGAAAGA | 63893 |
| rs77537806 | snp | G/T | 0.00199481 | 0.0315187 | upstream-variant-2KB, missense | AANAT, UBE2O | GRCh38.p7 | 17:76453122 | GGAGCTGCGGGCGTG[G/T]GGGCTGCGGGATCCG | 63893 |
| rs77554883 | in-del | -/TT | 0.271972 | 0.249033 | intron-variant | UBE2O | GRCh38.p7 | 17:76421402 | GACGGAGTTTCGCTC[-/TT]GTTGCCCAGGCTGGA | 63893 |
| rs77704090 | in-del | -/A | | | intron-variant | UBE2O | GRCh38.p7 | 17:76393303 | GGAGTATAGCTCTGT[-/A]CCCCAGGCTGGAGTG | 63893 |
| rs77720790 | snp | C/T | 0.030278 | 0.119257 | intron-variant | UBE2O | GRCh38.p7 | 17:76430222 | TCCCATTCTGTGTCC[C/T]TGTGGGTTTATACAT | 63893 |
| rs77846210 | snp | A/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76431657 | GGAAAAGAAAGACTA[A/T]TAGGGCCAGACACTG | 63893 |
| rs77897154 | snp | C/T | 0.0275645 | 0.114116 | intron-variant | UBE2O | GRCh38.p7 | 17:76416132 | ATATACATATATGTG[C/T]GTGTATAGATATATA | 63893 |
| rs77940351 | snp | A/G | 0.0193772 | 0.0965046 | intron-variant | UBE2O | GRCh38.p7 | 17:76410641 | AGGGCAGAGGGCAAC[A/G]TGGCAGGAGGCTGGG | 63893 |
| rs78004313 | snp | A/G | 0.0182019 | 0.0936463 | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390729 | ATTTTCTTTGCCACA[A/G]GGGACCCGCCTGTTG | 63893 |
| rs78074143 | snp | A/T | 0 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76419309 | AAAAAAAAAAAAAAA[A/T]CCCTTTCTCCTGAAA | 63893 |
| rs78258275 | snp | A/G | 0.0391387 | 0.134304 | intron-variant | UBE2O | GRCh38.p7 | 17:76440118 | CAGGTAATGCCAGGT[A/G]CTATGAGGGAAAAAA | 63893 |
| rs78328144 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76408916 | TTTCAACTGTCCTCA[C/T]GGGCTCTGAAATTCT | 63893 |
| rs78352481 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE2O | GRCh38.p7 | 17:76397338 | GGAGAGGAGAGCTGG[A/G]CTGTGTGGCTCCAAC | 63893 |
| rs78401039 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76450524 | ACAATGACAAAATAC[C/G]ACCACCGAGCCACAA | 63893 |
| rs78411046 | snp | C/G | 0.00140537 | 0.0264709 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76392012 | GTAGCAGAAGTGGGG[C/G]GGCACGGCTGGGTAG | 63893 |
| rs78462274 | snp | C/T | 0.0452528 | 0.143452 | intron-variant | UBE2O | GRCh38.p7 | 17:76432487 | AACCCCTTTCTCATC[C/T]TAGGATGCTTGTGGA | 63893 |
| rs78488375 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | UBE2O | GRCh38.p7 | 17:76426328 | TTCTACTCTACTTGA[C/T]GTAGTTGGGCTGGAT | 63893 |
| rs78560743 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76389701 | CACGGTGTGTGGTCC[A/G]GCTCCATCCTCCCGC | 63893 |
| rs78597487 | in-del | -/AAAA | | | splice-donor-variant, downstream-variant-500B | UBE2O | GRCh38.p7 | 17:76389528 | AAAAAAAAAAAAAAA[-/AAAA]TGCAAGTAAAAAAAA | 63893 |
| rs78701971 | in-del | -/TT | | | intron-variant | UBE2O | GRCh38.p7 | 17:76395372 | ATTTTTTTTTTTTTT[-/TT]AGTGGAGACGGGGTT | 63893 |
| rs78800379 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76442085 | TCAAGTGCTTTAGGC[A/G]GGGTTCTTACAGGGG | 63893 |
| rs79012277 | snp | A/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76404924 | TCCAATAATTTATTT[A/T]TTTAAAGAAATGTTA | 63893 |
| rs79094923 | snp | A/T | 0.0391387 | 0.134304 | intron-variant | UBE2O | GRCh38.p7 | 17:76418476 | AACAGTTGGAGGAAG[A/T]TTAGATATTCAATTC | 63893 |
| rs79228337 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | UBE2O | GRCh38.p7 | 17:76436460 | AGGCAAATAAGAGGA[C/T]GACTCCAGCAATTTT | 63893 |
| rs79289485 | snp | C/T | 0.00874735 | 0.0655527 | intron-variant | UBE2O | GRCh38.p7 | 17:76397112 | AGCATCTGTCCAAGG[C/T]GTTAGGGGACCTTGG | 63893 |
| rs79307215 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76450523 | TACAATGACAAAATA[C/T]CACCACCGAGCCACA | 63893 |
| rs79370127 | snp | A/C/T | 3.30852e-05 | 0.00406712 | intron-variant | UBE2O | GRCh38.p7 | 17:76397758 | CCGGCCCAAGTTGCC[A/C/T]TAGTCACAAGCTCAG | 63893 |
| rs79488198 | snp | C/T | 0.5 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76408974 | TATTGTCTAACATTT[C/T]TTTTTTTTTTTTGAG | 63893 |
| rs79975658 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76401963 | CGCCCCTTTTCTAGG[A/G]AACCGCTCTGTTTAG | 63893 |
| rs80111125 | snp | C/T | 0.0134861 | 0.0810011 | intron-variant | UBE2O | GRCh38.p7 | 17:76450203 | ATACTATCACCTTGA[C/T]GGAATTCATAAGGAG | 63893 |
| rs80264753 | snp | C/T | 0.5 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76408975 | ATTGTCTAACATTTC[C/T]TTTTTTTTTTTGAGA | 63893 |
| rs80317542 | snp | A/C | 0.00416364 | 0.0454366 | intron-variant | UBE2O | GRCh38.p7 | 17:76397907 | CTGGGCAAAGGGGAC[A/C]AAGTCAGGGGGCCCA | 63893 |
| rs80339342 | snp | A/C | 0 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76425230 | GTCCTTTCGACAAAA[A/C]AAAAAAAAAAAAAAA | 63893 |
| rs111275154 | snp | C/T | 0.0429648 | 0.14013 | intron-variant | UBE2O | GRCh38.p7 | 17:76416927 | AGTGAGACAAAGCTG[C/T]GGCTGGTCACATGGA | 63893 |
| rs111321090 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | UBE2O | GRCh38.p7 | 17:76424356 | TGGGATTACAAGTGT[A/G]AGCCACCACACTCTG | 63893 |
| rs111379781 | snp | G/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76421403 | ACGGAGTTTCGCTCT[G/T]GTTGCCCAGGCTGGA | 63893 |
| rs111401658 | snp | C/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76436023 | AGGCTGAGACGGGCG[C/G]ATCACCTGAGCTCAG | 63893 |
| rs111414508 | snp | A/T | 0.0142736 | 0.0832652 | intron-variant | UBE2O | GRCh38.p7 | 17:76437286 | AAACCCCGTCTCTAC[A/T]AAAAATACACAAAAT | 63893 |
| rs111515289 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE2O | GRCh38.p7 | 17:76441560 | CTAAAACTGAACCCA[C/T]TGACATCAACGAGGT | 63893 |
| rs111545387 | snp | A/G | 0.5 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76449688 | CTTTGGGAGGCCGAG[A/G]CGGGCGGATCACCTG | 63893 |
| rs111559937 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76454910 | GGCGGGTGGGAGACC[C/T]GAGGTCAGGAGTTCA | 63893 |
| rs111565452 | snp | A/G | 1.71784e-05 | 0.00293069 | intron-variant | UBE2O | GRCh38.p7 | 17:76399039 | AACCCCACCCCCTCC[A/G]CGGAAAGGGCAGAGA | 63893 |
| rs111720793 | in-del | -/A | 0 | 0 | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76454323 | CTACTAAAAATACGG[-/A]AAAAAAAAAAAAATA | 63893 |
| rs111743827 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | UBE2O | GRCh38.p7 | 17:76431486 | GCACTCCAGCCTGGG[C/T]GACAGGGTGCTCTGT | 63893 |
| rs111783470 | snp | A/G | 0.5 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76416129 | CATATATACATATAT[A/G]TGCGTGTATAGATAT | 63893 |
| rs111831863 | snp | G/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76421402 | GACGGAGTTTCGCTC[G/T]TGTTGCCCAGGCTGG | 63893 |
| rs112073899 | snp | A/G | 0.00591345 | 0.0540533 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76396756 | ATCCGAGGATGCCCC[A/G]CTGGTGCTGCCTTCT | 63893 |
| rs112083891 | snp | C/T | 0.00597247 | 0.0543191 | intron-variant | UBE2O | GRCh38.p7 | 17:76422864 | TGGGCACCAGTGCAC[C/T]CCAGCAAGTGCCTGG | 63893 |
| rs112100699 | snp | C/T | 0.271702 | 0.249056 | intron-variant | UBE2O | GRCh38.p7 | 17:76424129 | TAGCCAGGATGGTCT[C/T]GATCTCCTGACCTTG | 63893 |
| rs112106835 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76400949 | GAAGGAAAGGGGCAG[C/T]AGCTCAGCTCCAGGG | 63893 |
| rs112150759 | snp | C/T | 0.0425829 | 0.139564 | intron-variant | UBE2O | GRCh38.p7 | 17:76414673 | GAGGCACAGCCTGCC[C/T]GAGGGACAGAGAAAG | 63893 |
| rs112156102 | in-del | -/A | 0.5 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76403491 | GCCCAAGCTGGTCTT[-/A]AAACTCTTGAGCTCA | 63893 |
| rs112198174 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76424776 | TGAGCTATGATCGAG[C/T]CACTGCACTCCAGCC | 63893 |
| rs112274713 | snp | A/G | 0.0142736 | 0.0832652 | intron-variant | UBE2O | GRCh38.p7 | 17:76437300 | CTAAAAATACACAAA[A/G]TTAGCCGGGCGTGGT | 63893 |
| rs112340103 | snp | C/G | 0.081446 | 0.184634 | intron-variant | UBE2O | GRCh38.p7 | 17:76429468 | AAGTGCTTCAGCCTG[C/G]GAGGCAGAGGTTGCA | 63893 |
| rs112478889 | snp | C/T | 0.0498117 | 0.149749 | intron-variant | UBE2O | GRCh38.p7 | 17:76415990 | GTATACATATGCACA[C/T]ACACGTATATACGTA | 63893 |
| rs112558571 | snp | C/G | 0.0126979 | 0.078662 | intron-variant | UBE2O | GRCh38.p7 | 17:76411842 | AGGCACATGCCACCA[C/G]CCGGCTAATTTTATT | 63893 |
| rs112661427 | snp | C/G | 0.5 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76442963 | ACTGATGACAAGTTA[C/G]AATGAGGGCCAAAGA | 63893 |
| rs112699830 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76414820 | CTTGGCGGCAGGAGC[C/T]GGGAGCCGAGGAGCC | 63893 |
| rs112750934 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | UBE2O | GRCh38.p7 | 17:76410449 | AGGACATCCCTCAAC[A/G]AAGAATGGCGTGGCC | 63893 |
| rs112760762 | snp | C/T | 0.5 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76421906 | GAAAAGACAAGATGA[C/T]GCCACCAGACTGCAT | 63893 |
| rs112775865 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76392218 | CCCAGGACACTGTGC[A/G]GATCACGCAGGAAGA | 63893 |
| rs112804351 | in-del | -/G | 0.061536 | 0.16426 | intron-variant | UBE2O | GRCh38.p7 | 17:76397775 | GTCACAAGCTCAGCA[-/G]GGGGGGTCTTGCCAG | 63893 |
| rs112823298 | snp | A/G | 0.0205511 | 0.0992634 | intron-variant | UBE2O | GRCh38.p7 | 17:76409436 | GAGTCTCGCTTTGTC[A/G]CCCAGGTTGGAGTGC | 63893 |
| rs112867362 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | UBE2O | GRCh38.p7 | 17:76443437 | GGGATCACAGGCACC[C/T]ACCACCACGCATGGC | 63893 |
| rs112871788 | snp | A/G | 0.00835141 | 0.0640778 | intron-variant | UBE2O | GRCh38.p7 | 17:76440703 | AGCAGAGGTGGGAAA[A/G]CTACAGCCTGCAGGT | 63893 |
| rs112953050 | snp | A/T | 0.0185938 | 0.0946107 | intron-variant | UBE2O | GRCh38.p7 | 17:76424876 | TTATTTTTTATTTTT[A/T]TTTTTTGAGACAGAG | 63893 |
| rs113000996 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | UBE2O | GRCh38.p7 | 17:76420726 | GGAAGAGACACAAGA[C/T]GTCCTGGGATCGAGT | 63893 |
| rs113122326 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | UBE2O | GRCh38.p7 | 17:76429205 | GCGTCCAGCCAGCCC[C/T]CTACTATGTTTGCAA | 63893 |
| rs113169769 | snp | A/C | 0.5 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76402759 | TTCATGTCCAGGGCA[A/C]AGATTCCTCTATGCC | 63893 |
| rs113232095 | snp | C/T | 0.00237615 | 0.0343865 | intron-variant | UBE2O | GRCh38.p7 | 17:76405345 | GAGACATGCAAGTCC[C/T]GTGGTGCAGCAGCCC | 63893 |
| rs113302314 | snp | C/G | 0.5 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76397198 | GGCCTGTGTGGGGAG[C/G]TGGGAACATATGACA | 63893 |
| rs113344261 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76401875 | TGAGACTCTGTCTCA[A/C]AAAAAAAAAAAAAAA | 63893 |
| rs113426621 | in-del | -/T | 0.5 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76450618 | GCCTCAAAGTTGTTG[-/T]TTTTTTTTTTCTTTT | 63893 |
| rs113556863 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | UBE2O | GRCh38.p7 | 17:76429062 | GCATGCCACCATGCC[C/T]GGCTAATTTTTGTAT | 63893 |
| rs113607172 | snp | A/T | 0.5 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76424863 | TCTTTTTTTTTTTTT[A/T]TTTTTTATTTTTTTT | 63893 |
| rs113626400 | in-del | -/GGCTTA | 0.5 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76449305 | GGGGCAAGGCACTGT[-/GGCTTA]GGCTTATGCCTGTAA | 63893 |
| rs113731509 | in-del | -/GT | 0.0535932 | 0.154675 | intron-variant | UBE2O | GRCh38.p7 | 17:76416172 | CATACGTGTGTGTGT[-/GT]ATATGTATATGTGTA | 63893 |
| rs113841636 | snp | G/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76417708 | CCTTCGACTACAGGA[G/T]GAAAGAATGCTAAGC | 63893 |
| rs113908307 | snp | A/G | 7.16846e-05 | 0.00598641 | intron-variant | UBE2O | GRCh38.p7 | 17:76399937 | CTGCAAGGGCGGAGC[A/G]GAGAGGACAGGGCTG | 63893 |
| rs113934814 | snp | C/G | 0.0448719 | 0.142907 | intron-variant | UBE2O | GRCh38.p7 | 17:76412741 | TCGGCCGGGCGCAGT[C/G]GCTCAAGCCTGTAAT | 63893 |
| rs113983361 | snp | A/G | 0.5 | 0 | intron-variant | UBE2O | GRCh38.p7 | 17:76442826 | TGTTCACTGGTTGAA[A/G]GAGGACTAGAGGCAG | 63893 |
| rs114075283 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | UBE2O | GRCh38.p7 | 17:76447113 | GTACCTCCTATTACA[C/T]TAAGACTTTCAACTG | 63893 |
| rs114076002 | snp | C/T | 0.00438332 | 0.0466095 | intron-variant | UBE2O | GRCh38.p7 | 17:76409762 | CCCAGGACCGACATC[C/T]TCTGTGCCTCCTCTG | 63893 |
| rs114107891 | snp | A/C/G | 0.00486551 | 0.0490836 | missense | UBE2O | GRCh38.p7 | 17:76398272 | CATCCTCCTTGTGAG[A/C/G]AGCCCCATCCTCAGT | 63893 |
| rs114112291 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | UBE2O | GRCh38.p7 | 17:76429824 | CTTTTAGTGTGCAGA[C/T]GTTCATGAATCCCTC | 63893 |
| rs114161260 | snp | G/T | 0.0205511 | 0.0992634 | intron-variant | UBE2O | GRCh38.p7 | 17:76417125 | TGAGCTCCAGGCCCT[G/T]CCGGCTACAGCTCCA | 63893 |
| rs114205580 | snp | A/G | 0.00098811 | 0.0222054 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76399664 | TGCCGAGTGCAGCCT[A/G]TCATCTCTGCCTTCT | 63893 |
| rs114283460 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76434227 | ATAGACCTAGACATA[C/G]ATGGAAACCCAGCAC | 63893 |
| rs114283949 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE2O | GRCh38.p7 | 17:76403718 | AGCATCCAGATCTTG[A/G]GTTTTAAAAATACCA | 63893 |
| rs114546961 | snp | A/G | 0.00597247 | 0.0543191 | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76389975 | TAAACCTCTGGGCCT[A/G]TCTCTGGGCACTAGG | 63893 |
| rs114630695 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBE2O | GRCh38.p7 | 17:76438168 | AGAAAAGGTTTTTCT[A/G]AAAGCTATAAAACTT | 63893 |
| rs114680846 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBE2O | GRCh38.p7 | 17:76436594 | GGCCCCTGCCCTGCA[C/T]GCTGTCCCTCGCCTG | 63893 |
| rs114806992 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | UBE2O | GRCh38.p7 | 17:76434010 | CTCACCAGAAGACAA[A/C]AACGAGCCCTCCTAA | 63893 |
| rs114864549 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UBE2O | GRCh38.p7 | 17:76404574 | AAAGAGTAGTGTTGG[A/G]ACAACTGCATGTGGT | 63893 |
| rs114972114 | snp | C/T | 0.0209421 | 0.100162 | intron-variant | UBE2O | GRCh38.p7 | 17:76429851 | CCTCTTTCAGTCCAG[C/T]GTTACCCTGCCCCTT | 63893 |
| rs115127740 | snp | C/T | 0.0267878 | 0.112589 | intron-variant | UBE2O | GRCh38.p7 | 17:76447055 | CACTGGCACAACTTC[C/T]ACCTATCCCAACATC | 63893 |
| rs115247230 | snp | C/T | 0.0252325 | 0.109451 | intron-variant | UBE2O | GRCh38.p7 | 17:76439533 | TGCTCTGATGGCCAA[C/T]AGAATGTATGCCCAG | 63893 |
| rs115247474 | snp | A/C | 0.00914312 | 0.0669923 | intron-variant | UBE2O | GRCh38.p7 | 17:76413094 | GAAACCTTGCTGAGG[A/C]CTAGGATCCCACTTT | 63893 |
| rs115302030 | snp | C/G | 0.00636936 | 0.0560724 | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76451664 | GCCCTCCCCTGAAAT[C/G]AGACCTCTCAACCTC | 63893 |
| rs115337520 | snp | A/G | 0.0168055 | 0.0901129 | intron-variant | UBE2O | GRCh38.p7 | 17:76433841 | AGCCTGGGCAACATA[A/G]TGAGATGGTGACTCT | 63893 |
| rs115350769 | snp | A/C/G | 0.0182284 | 0.0939223 | intron-variant | UBE2O | GRCh38.p7 | 17:76438217 | TATTTAATTGAGACA[A/C/G]AGTTTCAGTGGGGAA | 63893 |
| rs115410915 | snp | C/T | 0.0166325 | 0.0896639 | intron-variant | UBE2O | GRCh38.p7 | 17:76435637 | GAAGGTGATCTCGTG[C/T]AATCCCCAGTAACTA | 63893 |
| rs115428223 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBE2O | GRCh38.p7 | 17:76394486 | CATCCTATTTTGCAG[A/G]TAAAAAGGAAGAAAC | 63893 |
| rs115555751 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | UBE2O | GRCh38.p7 | 17:76435849 | ACACCCCGGCACAGA[A/G]GGGACAGAAAACAGT | 63893 |
| rs115566409 | snp | C/T | 0.00636936 | 0.0560724 | intron-variant | UBE2O | GRCh38.p7 | 17:76446998 | ATGCAGTGTTCCTCC[C/T]GTCCTGCTCCCTACC | 63893 |
| rs115720352 | snp | C/T | 0.0225045 | 0.103662 | intron-variant | UBE2O | GRCh38.p7 | 17:76437881 | GCAATTATGAGGTTA[C/T]GAAATAGGACAGCAA | 63893 |
| rs115767481 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBE2O | GRCh38.p7 | 17:76406107 | CTCCTGACCAGCTGC[A/G]GCCTGCACCTTATCT | 63893 |
| rs115768156 | snp | G/T | 0.029116 | 0.117091 | intron-variant | UBE2O | GRCh38.p7 | 17:76420436 | ATACCTGTGATTTTA[G/T]ATCAATCCCAGTGGC | 63893 |
| rs116067292 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | UBE2O | GRCh38.p7 | 17:76430244 | TTTATACATCTAAAA[A/C]CAATTATTTTGCTGT | 63893 |
| rs116077227 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | UBE2O | GRCh38.p7 | 17:76395640 | CCAGTCAGCCCCGGA[A/G]GTTTGGGGACCCAAG | 63893 |
| rs116202300 | snp | G/T | 0.0174175 | 0.0916809 | intron-variant | UBE2O | GRCh38.p7 | 17:76407759 | GAGGCTGGCAGGGCA[G/T]GCAGTGCCCAGTGCT | 63893 |
| rs116252102 | snp | C/G | 0.0107246 | 0.0724382 | intron-variant | UBE2O | GRCh38.p7 | 17:76440709 | GGTGGGAAAACTACA[C/G]CCTGCAGGTCATGTC | 63893 |
| rs116322643 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | UBE2O | GRCh38.p7 | 17:76416184 | TACGTGTGTGTGTGT[A/G]TATGTATATGTGTAT | 63893 |
| rs116330430 | snp | A/C/T | 0.00129357 | 0.0253998 | intron-variant | UBE2O | GRCh38.p7 | 17:76396102 | GAAGGCGGGGGAAGG[A/C/T]GAAGACCAGGCAAGG | 63893 |
| rs116424469 | snp | C/T | 0.0232847 | 0.105357 | intron-variant | UBE2O | GRCh38.p7 | 17:76411603 | GAAGGCCAAACAGGA[C/T]GAGACATGGGTGCTC | 63893 |
| rs116515291 | snp | A/G | 0.046775 | 0.145601 | intron-variant | UBE2O | GRCh38.p7 | 17:76404715 | TCCGGGGTGGGTGAC[A/G]GGGCATCACATCTAT | 63893 |
| rs116565085 | snp | A/G | 0.0402882 | 0.136092 | intron-variant | UBE2O | GRCh38.p7 | 17:76446041 | GTGATAGCCTCTTGT[A/G]AACTGGAAAGCACAT | 63893 |
| rs116577165 | snp | A/G | 0.00953873 | 0.0683987 | intron-variant | UBE2O | GRCh38.p7 | 17:76419491 | AATAACTAAGAAAGC[A/G]AGAGTTGACTGATGC | 63893 |
| rs116720041 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76408289 | GCCTCATGCTAACCA[C/G]GTGCTTCCTACCTGG | 63893 |
| rs116822421 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | UBE2O | GRCh38.p7 | 17:76403988 | AAAACAGAAATCTCT[A/G]AGTCCATACTGATAA | 63893 |
| rs116879618 | snp | C/T | 0.00909159 | 0.0668067 | upstream-variant-2KB, synonymous-codon | AANAT, UBE2O | GRCh38.p7 | 17:76452767 | GCCCTCCGGGTACCA[C/T]TGGACGCGCACGTAG | 63893 |
| rs116987939 | snp | A/G | 0.0872718 | 0.189788 | intron-variant | UBE2O | GRCh38.p7 | 17:76440349 | TTTACTTTGAGACAG[A/G]GTCTTGCTCTGTTGC | 63893 |
| rs117065023 | snp | C/G | 0.0115144 | 0.0749975 | intron-variant | UBE2O | GRCh38.p7 | 17:76431837 | AAACTCCCCCAGACA[C/G]CTGAAAGGGCCACAC | 63893 |
| rs117222678 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76406311 | CCTGCGTCTTTTTTA[A/G]CTGGTTCCTCAAACC | 63893 |
| rs117233817 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | UBE2O | GRCh38.p7 | 17:76449191 | GAGACTAAGATTAAG[C/G]CTTTACTCATTGCCC | 63893 |
| rs117258449 | snp | C/T | 0.0356815 | 0.128715 | intron-variant | UBE2O | GRCh38.p7 | 17:76416020 | ATGTGTATACATATG[C/T]ACACACACGTATATA | 63893 |
| rs117327671 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76439124 | AGGGGCAGCTGACGG[C/T]GTGGTTTGGAGGCGC | 63893 |
| rs117339093 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE2O | GRCh38.p7 | 17:76446125 | AACTCCCCATCGCCA[C/T]CCAGAAGCAGGCTAA | 63893 |
| rs117404980 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE2O | GRCh38.p7 | 17:76407779 | TGCCCAGTGCTCCCA[A/G]GAGAGGGAGGCTGGC | 63893 |
| rs117431565 | snp | A/C | 0.00159617 | 0.0282053 | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390002 | TAGGAGAGCCCCCGC[A/C]GGCCGTCCCCTTCGG | 63893 |
| rs117445007 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76451320 | TGTTGCACAAAAGTA[A/G]TATTTTCCAAATACT | 63893 |
| rs117544870 | snp | G/T | 0.100231 | 0.200173 | intron-variant | UBE2O | GRCh38.p7 | 17:76419124 | CCCTATCTCTACAGA[G/T]TTTTTTTTTTTAAAT | 63893 |
| rs117592864 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76442227 | CCAAAGTAGTAACTA[C/T]AATATGGTGTATTCT | 63893 |
| rs117717596 | snp | C/T | 0.00716266 | 0.059414 | intron-variant | UBE2O | GRCh38.p7 | 17:76441878 | ATAGCCACTGCAACT[C/T]CAGGCCCCGCCCCCA | 63893 |
| rs117849139 | snp | C/T | 0.00914312 | 0.0669923 | intron-variant | UBE2O | GRCh38.p7 | 17:76444454 | AGGTGGGAGCACTGC[C/T]TGAGCCCAGGAGGCG | 63893 |
| rs117983706 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76444982 | CCACACACACAGTCC[A/G]CTGAATCTGCCGGTC | 63893 |
| rs118045327 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76394325 | CCAGTAAGGGACTGC[A/G]GAGTCAACAAGGTGG | 63893 |
| rs118057296 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | UBE2O | GRCh38.p7 | 17:76433175 | GAATAGCCAAAAGGT[A/G]AAAATGACACAACAA | 63893 |
| rs118164903 | snp | A/G | 0.0327778 | 0.123752 | intron-variant | UBE2O | GRCh38.p7 | 17:76435150 | GCAAACGGGAAGGTC[A/G]GGATCCAGATCCAGG | 63893 |
| rs118176284 | snp | G/T | 0.0134861 | 0.0810011 | intron-variant | UBE2O | GRCh38.p7 | 17:76413600 | ATATAAAATGTGTAT[G/T]TTACCGTGAGTGACT | 63893 |
| rs137873848 | snp | C/G | 1.64751e-05 | 0.00287007 | missense | UBE2O | GRCh38.p7 | 17:76402665 | ACCTTCCCCAGCCAG[C/G]AGTCATAGGCAATGT | 63893 |
| rs137956692 | snp | A/G | 0.000131833 | 0.00811782 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76396285 | CTCCTTGCGCTCTAC[A/G]TCGGGCACTGCTTCC | 63893 |
| rs137957104 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76441953 | GATTCATTTGCAGTC[A/G]GGTGGGGCATTCTTT | 63893 |
| rs137965500 | snp | C/T | 0.000214149 | 0.0103455 | missense | UBE2O | GRCh38.p7 | 17:76398293 | CATCCTCAGTATTGC[C/T]GATGCGGATGACGAT | 63893 |
| rs137979989 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | UBE2O | GRCh38.p7 | 17:76448275 | TGATCCTATCTGAAT[A/G]AAACGCAATTTAGAT | 63893 |
| rs138072910 | in-del | -/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76426522 | CTTTTAGACAAATGA[-/C]CCTAGTTTTAAAATT | 63893 |
| rs138171021 | in-del | -/C | 0.0197687 | 0.0974348 | intron-variant | UBE2O | GRCh38.p7 | 17:76445299 | ATAGTCAGACTGTTT[-/C]CCAGGTATAGTTATG | 63893 |
| rs138192575 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76436605 | TGCACGCTGTCCCTC[A/G]CCTGCTGCTGCTCTG | 63893 |
| rs138251834 | snp | C/T | 0.00795532 | 0.062565 | intron-variant | UBE2O | GRCh38.p7 | 17:76416187 | GTGTGTGTGTGTATA[C/T]GTATATGTGTATATG | 63893 |
| rs138254128 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | UBE2O | GRCh38.p7 | 17:76422934 | TGAAGGAAAAGCCAT[C/G]GGAATTGGGAACAAG | 63893 |
| rs138374346 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76394761 | GAGAAAGGGAAGTGA[C/G]GTCTGGTCAAAGGCA | 63893 |
| rs138410942 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76405720 | TATCTTCACAGACCG[A/C]ACACACCTCCGACCA | 63893 |
| rs138443715 | snp | G/T | 0.00159617 | 0.0282053 | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390602 | GAACCGGCCCAGAGA[G/T]CCCCGCGGCAGGCCC | 63893 |
| rs138587388 | snp | A/T | 0.000957222 | 0.0218562 | missense | UBE2O | GRCh38.p7 | 17:76391485 | GCCGCACCAGCTGGG[A/T]CATGGACTGCACCAC | 63893 |
| rs138590244 | snp | A/G | 0.00130737 | 0.0255338 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76405272 | GCCGATGAGCTTGAC[A/G]GCACAGTCGATGTTG | 63893 |
| rs138619735 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76436021 | GGAGGCTGAGACGGG[C/T]GGATCACCTGAGCTC | 63893 |
| rs138631138 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBE2O | GRCh38.p7 | 17:76445587 | GCCTACCTGTGTCTA[A/G]GGGTGACCTGGACAA | 63893 |
| rs138639662 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | UBE2O | GRCh38.p7 | 17:76414752 | TTGGCCTGGCAGGGG[G/T]CCAGCGGGCTGGTCT | 63893 |
| rs138693412 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76433337 | TAAATAAATCAGTCA[C/T]GAAGGCCACATCTAG | 63893 |
| rs138721928 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBE2O | GRCh38.p7 | 17:76409943 | GCCAGCAGAGGGAGA[A/G]CACAGTGAAGAATTT | 63893 |
| rs138786675 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBE2O | GRCh38.p7 | 17:76415064 | CTACCTAACCAGTGG[C/T]CCCGGACTGCTCCAT | 63893 |
| rs138829004 | in-del | -/GGGG | | | intron-variant | UBE2O | GRCh38.p7 | 17:76407529 | GCACCATGTGTGGCA[-/GGGG]GGAGGGCTGCCTCCA | 63893 |
| rs138913325 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76400017 | TGACAGCTGTATACA[C/T]CTGAGTAGCCGGCAA | 63893 |
| rs138922387 | snp | A/G | 0.040671 | 0.13668 | intron-variant | UBE2O | GRCh38.p7 | 17:76431441 | GAATTGCTTGAATCC[A/G]GGAGGCACAGGTTGC | 63893 |
| rs138988964 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76427019 | TTTCCTTAGCACACT[A/G]AAGATTTTACTTCCT | 63893 |
| rs139026939 | snp | C/G | 0.0023933 | 0.0345097 | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76389624 | ACAATGCACTGGGAA[C/G]CACAGCCCCACCAGT | 63893 |
| rs139170814 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76402806 | GGGGGAGGATCTAGA[C/G]AGCTCACTGACTGGA | 63893 |
| rs139196411 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76421028 | AAATACAAACACATA[A/G]CAGCATGTATTTGGG | 63893 |
| rs139277198 | snp | C/T | 0.000562467 | 0.0167606 | missense | UBE2O | GRCh38.p7 | 17:76391155 | CCGATGCGTCTGGTG[C/T]GGTCTCCGAAGTCTG | 63893 |
| rs139315841 | snp | A/G | 0.000167683 | 0.00915496 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76392069 | GTAGAGGCCATCCTC[A/G]TAGGGGGTTCGAGTG | 63893 |
| rs139324747 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76416419 | CCAGAGAAACAGCTA[A/G]AAGGGACTGCATCCC | 63893 |
| rs139441211 | snp | A/G | 1.66219e-05 | 0.00288283 | intron-variant | UBE2O | GRCh38.p7 | 17:76391850 | CAATTCTGTTCCCCA[A/G]GCCCCTATCCACCAG | 63893 |
| rs139476705 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76403127 | CACATCAAGGATATC[A/G]AGAGCCAAGTCCCTC | 63893 |
| rs139511874 | snp | A/G | 0.000399281 | 0.0141238 | utr-variant-5-prime, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76453689 | ACGTGTAGAGCATAT[A/G]TATAATGCACTGTAT | 63893 |
| rs139572215 | snp | C/T | 0.00478085 | 0.0486577 | intron-variant | UBE2O | GRCh38.p7 | 17:76437318 | AGCCGGGCGTGGTGG[C/T]GGGCACCTGTAGTCC | 63893 |
| rs139605465 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76407037 | TGCCCAGTCCTTAAA[C/T]GCAGGGTTCTTGAGT | 63893 |
| rs139654746 | in-del | -/AT | 0.0115144 | 0.0749975 | utr-variant-5-prime, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76453684 | AGATACGTGTAGAGC[-/AT]ATATGTATAATGCAC | 63893 |
| rs139694108 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | UBE2O | GRCh38.p7 | 17:76407335 | GCCACTTTTCTAAAT[C/G]AAAGAATATTCTGTG | 63893 |
| rs139697578 | snp | A/G | 8.2513e-05 | 0.00642259 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76398955 | CTGCCACATCACGTC[A/G]GCTGAGGTCATCGTG | 63893 |
| rs139744095 | in-del | -/GG | | | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76451775 | GGGGTGTGAGATACA[-/GG]GGGGTGTGTGTGTGT | 63893 |
| rs139752037 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76392648 | GTTTTTCCTCATAAA[C/T]CATTACTTTAAGACT | 63893 |
| rs139799121 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76418413 | CTGCGAGGCGCCATT[C/T]GGCTGTCTGCACCCT | 63893 |
| rs139858351 | snp | A/C | 0.0244538 | 0.107838 | intron-variant | UBE2O | GRCh38.p7 | 17:76423802 | AATTGATAGAGGTGG[A/C]CTACGGCACAGTGTC | 63893 |
| rs139968373 | snp | A/G | 5.05497e-05 | 0.00502716 | missense | UBE2O | GRCh38.p7 | 17:76391319 | GCTGGGGGCTCTGGC[A/G]AGCTGCTGGCCTTGG | 63893 |
| rs139978352 | snp | G/T | 0.00438332 | 0.0466095 | intron-variant | UBE2O | GRCh38.p7 | 17:76446307 | AGGACTGTTGTGCTG[G/T]CAATTCATGTTATAC | 63893 |
| rs139988070 | snp | A/G | 8.24559e-05 | 0.00642037 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76396225 | CAGCACCGGGGTTTC[A/G]CTGGGCCACTCAGCC | 63893 |
| rs140008195 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76437931 | GGGGACAGGCTAAAT[A/G]CACGCTTCGAAGGGA | 63893 |
| rs140008685 | snp | A/G/T | 1.64749e-05 | 0.00287005 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76399625 | GTCCGTGTCATCAGC[A/G/T]GCCTCATCATCTGCG | 63893 |
| rs140055538 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76407727 | AGCTGGTGAAAGCTG[G/T]CATCATGGCAAGGCC | 63893 |
| rs140057447 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76451865 | AACCCGGGTTCAAGG[C/T]TTCGGGTTTATGATG | 63893 |
| rs140094896 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE2O | GRCh38.p7 | 17:76447222 | TGATCTCTGAATCCT[A/G]AACTTAAGTATTCTC | 63893 |
| rs140098625 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76410768 | CTGCCAGGAGCACTC[C/T]CCCTCCACGGCTGCC | 63893 |
| rs140175779 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE2O | GRCh38.p7 | 17:76410741 | GCCGGGGAAGCTCAC[C/T]GGGGGCCTCTCCTGC | 63893 |
| rs140233675 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76425092 | TAGCCAGGATGGTCT[C/T]GATCTCCTGACCTCG | 63893 |
| rs140317141 | snp | C/T | 0.0111196 | 0.0737302 | intron-variant | UBE2O | GRCh38.p7 | 17:76414753 | TGGCCTGGCAGGGGG[C/T]CAGCGGGCTGGTCTC | 63893 |
| rs140399157 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76448073 | ACAGCCAGGAAGAGC[A/G]CCCAAGGGTTTTGGC | 63893 |
| rs140512067 | snp | C/T | 0.16618 | 0.23553 | intron-variant | UBE2O | GRCh38.p7 | 17:76393236 | GCACTCCAGCCTGGG[C/T]GACAGAGTGAGACCC | 63893 |
| rs140513072 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76398755 | GCTCTGACCCCAGAT[C/G]CACTGCCCATTCTCC | 63893 |
| rs140592240 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBE2O | GRCh38.p7 | 17:76428955 | CGCCCAGGCTGGAGT[A/G]CAGTGGCATGATCTT | 63893 |
| rs140600896 | snp | A/C/G | 5.05364e-05 | 0.00502654 | missense | UBE2O | GRCh38.p7 | 17:76402080 | GAGTCGCTGACGTGC[A/C/G]GGCAGACGTCGTAGA | 63893 |
| rs140710618 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76394560 | AGATGATGTGTACGA[C/T]GACATATTCTGTGTG | 63893 |
| rs140727778 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE2O | GRCh38.p7 | 17:76444941 | TCCCACCTGCACTAG[C/T]GGTGACCACACACAC | 63893 |
| rs140731654 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76435614 | CAGGTGCTGTGCTGA[A/G]CCCTCTCGAAGGTGA | 63893 |
| rs140919927 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76393396 | AGTCTCCTCACGCCC[A/G]GCTAATTTTTTGTAT | 63893 |
| rs140920831 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76412364 | CCCAAAGAGTAAAAA[C/T]AATCTGAGAAACGCC | 63893 |
| rs140923805 | snp | A/G | 0.00102736 | 0.0226412 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76405254 | ATAGATGATGCAGTT[A/G]GTGCCGATGAGCTTG | 63893 |
| rs141025514 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76448592 | AACCTGGTGAAACCC[G/T]GAATGTCATGGCAAC | 63893 |
| rs141048621 | snp | A/G | 0.00636936 | 0.0560724 | intron-variant | UBE2O | GRCh38.p7 | 17:76441135 | CTGGCCACTTTAAGG[A/G]AAGTGAGATGACACA | 63893 |
| rs141106159 | snp | A/G | 0.000153988 | 0.00877328 | missense | UBE2O | GRCh38.p7 | 17:76396664 | AGGGGTGGGATGGGG[A/G]GCTCCTCTATCTTGG | 63893 |
| rs141110856 | snp | C/T | 0.039522 | 0.134904 | intron-variant | UBE2O | GRCh38.p7 | 17:76414475 | GTCCTGTCTGGATGG[C/T]GGTGGGGGAAGGCAG | 63893 |
| rs141113432 | snp | C/G | 0.00914312 | 0.0669923 | intron-variant | UBE2O | GRCh38.p7 | 17:76399087 | TGTCCCTGTGGGCTT[C/G]GTAACCTGAAACTCT | 63893 |
| rs141149163 | snp | A/G | 0.0356815 | 0.128715 | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76454988 | AAAAATTAGCCGGGC[A/G]CGGTGGCAGCCGCCT | 63893 |
| rs141224792 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76434883 | TCCTTCCACCTCCAT[C/T]GGTGGTACCTCTGGC | 63893 |
| rs141227791 | snp | C/T | 0.00835141 | 0.0640778 | intron-variant | UBE2O | GRCh38.p7 | 17:76444716 | CCATTTCCCCCAGTA[C/T]AGTGCTGGGATGACC | 63893 |
| rs141268814 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76442518 | TCCCAAGAGTCTGCA[C/T]GTGCGTGATAGCACA | 63893 |
| rs141373479 | snp | C/G/T | 4.9451e-05 | 0.00497227 | missense | UBE2O | GRCh38.p7 | 17:76398920 | TCGTTGGAGCGGATG[C/G/T]TGCATTCCACGGAGC | 63893 |
| rs141379339 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBE2O | GRCh38.p7 | 17:76402234 | CTAAATAGCACAATT[C/T]GTCTTCTACCATCAA | 63893 |
| rs141427097 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76431247 | CCGGCCACGGTGGCT[A/C]ATGCCTGTAATCCCA | 63893 |
| rs141551071 | snp | G/T | 0.00478085 | 0.0486577 | intron-variant | UBE2O | GRCh38.p7 | 17:76422859 | GGCACTGGGCACCAG[G/T]GCACCCCAGCAAGTG | 63893 |
| rs141583518 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76427925 | TCCAAACCTCTATTA[C/T]TGTTAGGGTCGATTT | 63893 |
| rs141637476 | snp | A/G | 4.94271e-05 | 0.00497102 | missense | UBE2O | GRCh38.p7 | 17:76396392 | GAAACTTCTTCTCCC[A/G]AGTTGGCTTCTCAGG | 63893 |
| rs141661948 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76417898 | TCCTCCCAGTCTCCA[A/T]GATGGTGCTGTTTCC | 63893 |
| rs141685226 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76423858 | GGAGACTTCCTCTCT[A/T]CACACCAGGTGGCTC | 63893 |
| rs141699867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76432877 | ATGCATGCCAAATCA[C/T]AATGCAATACCCATG | 63893 |
| rs141700513 | snp | A/G/T | 0.00067757 | 0.0183946 | synonymous-codon, missense | UBE2O | GRCh38.p7 | 17:76391473 | CCTCGGGGGGCCGCC[A/G/T]CACCAGCTGGGTCAT | 63893 |
| rs141764172 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76404292 | GACACCAACATGACC[A/C]GGGGTAAAAGTGAAC | 63893 |
| rs141810186 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76436792 | ACGCCTCTTAGGACA[A/G]AGTATAAAATGGGGA | 63893 |
| rs141828878 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76445929 | TGGGCAGCATTTAGA[C/T]CATGACCTTCTCCAG | 63893 |
| rs141995516 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76445874 | AAGATGAAGCAATTC[C/T]GAACGGGCACTCTTG | 63893 |
| rs142041683 | in-del | -/TG | | | intron-variant | UBE2O | GRCh38.p7 | 17:76416036 | ACACACACGTATATA[-/TG]TGTGTGTACATATGT | 63893 |
| rs142051853 | snp | A/G | 0.00597247 | 0.0543191 | intron-variant | UBE2O | GRCh38.p7 | 17:76447654 | CACAAAGTAACAGAG[A/G]TAGGAAGTTCATGAG | 63893 |
| rs142052486 | snp | A/T | 0.0267878 | 0.112589 | intron-variant | UBE2O | GRCh38.p7 | 17:76408446 | CAATGTCACAAGTAG[A/T]GGAGCTGGGACCTGA | 63893 |
| rs142214923 | in-del | -/G | 0.0150606 | 0.0854603 | intron-variant | UBE2O | GRCh38.p7 | 17:76446445 | GTATAACAGGAAAAT[-/G]AAAAAACAAAAACAA | 63893 |
| rs142272308 | snp | A/G | 0.00318978 | 0.0398085 | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390297 | TCCTGGGCGTCACCC[A/G]GAACCTAGCCTGGTC | 63893 |
| rs142414938 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE2O | GRCh38.p7 | 17:76415961 | CATATGCACATACAC[A/G]TATATACGTATGCGT | 63893 |
| rs142431589 | snp | A/G | 0.00506134 | 0.0500505 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76398294 | ATCCTCAGTATTGCC[A/G]ATGCGGATGACGATG | 63893 |
| rs142461783 | snp | A/G | 0.0023124 | 0.0339243 | missense | UBE2O | GRCh38.p7 | 17:76399855 | CCATGGAATGGTCCC[A/G]GGAACACTGGGTGTC | 63893 |
| rs142462313 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | UBE2O | GRCh38.p7 | 17:76421425 | CAGGCTGGAGTGCAA[G/T]GGCGTGATCTCGGCA | 63893 |
| rs142482394 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76403813 | CAAGATGAGCCTGGC[A/G]CATCTCATGCCAGAA | 63893 |
| rs142499121 | snp | C/T | 0.00557542 | 0.0525036 | intron-variant | UBE2O | GRCh38.p7 | 17:76413478 | GTGCATTAATATACA[C/T]GTGGTAAGAATAAGT | 63893 |
| rs142646862 | snp | C/T | 0.0150606 | 0.0854603 | intron-variant | UBE2O | GRCh38.p7 | 17:76424111 | GACGGGGTTTCACCA[C/T]GTTAGCCAGGATGGT | 63893 |
| rs142710644 | snp | A/G | 0.0236746 | 0.106192 | intron-variant | UBE2O | GRCh38.p7 | 17:76436149 | CTACTCAGGAGGCTG[A/G]GGCAGGAGAATTGCT | 63893 |
| rs142843663 | snp | A/C | 0.000370882 | 0.0136126 | missense | UBE2O | GRCh38.p7 | 17:76391338 | TGCTGGCCTTGGGCA[A/C]CCCGTTGGGCAGTGC | 63893 |
| rs142843966 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76433755 | GGGTTTCGGCCAGTG[C/T]GGTGGCCTGTAATGC | 63893 |
| rs142850772 | snp | G/T | 0.00874735 | 0.0655527 | intron-variant | UBE2O | GRCh38.p7 | 17:76393265 | CCTGTCTTTTATTTT[G/T]TGGCTTATGTGTTTT | 63893 |
| rs142896234 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE2O | GRCh38.p7 | 17:76407204 | GTGCTCAGCAAGGTC[A/G]GCAGCTGTGATCACT | 63893 |
| rs142897217 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE2O | GRCh38.p7 | 17:76434465 | AAACTGTAAAGGACA[C/T]GCCAATAGTCCTGCC | 63893 |
| rs143045605 | snp | A/G | 0.000289929 | 0.0120366 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76391975 | ACAGGTTGGGGTTCA[A/G]GCGGCCACTGCATTG | 63893 |
| rs143060633 | snp | A/G | 0.000115698 | 0.00760496 | missense | UBE2O | GRCh38.p7 | 17:76395861 | TTAAAAGAATGATTT[A/G]CTAGAGGGGGGAAGA | 63893 |
| rs143081034 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBE2O | GRCh38.p7 | 17:76435960 | TCAAATTCTCATCAT[C/T]GTTAGGCCCCGTGCG | 63893 |
| rs143098527 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76426363 | AATTCTCTCAGAATG[C/T]TGCAGGATTTGCTCT | 63893 |
| rs143102468 | snp | A/G | 0.0178098 | 0.0926698 | intron-variant | UBE2O | GRCh38.p7 | 17:76408735 | GGTGCCAGCCGGCCT[A/G]GCAGGTGAACACTAG | 63893 |
| rs143126252 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76455086 | GAGCCTAGATCGCGC[C/T]GCTGCACTCCAGCCT | 63893 |
| rs143143875 | snp | A/G | 0.0225045 | 0.103662 | intron-variant | UBE2O | GRCh38.p7 | 17:76419863 | TGGCTCTACCCACGC[A/G]GAAACCTCAGAGTCT | 63893 |
| rs143191660 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76442198 | TCTGCCTGGGGAGCC[C/T]GCGACGGAAGTTGCC | 63893 |
| rs143276039 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | UBE2O | GRCh38.p7 | 17:76450692 | AATGGTGCCATCTCA[A/G]CTCACCGCAACCTCC | 63893 |
| rs143377135 | snp | A/G | 0.0193772 | 0.0965046 | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76389588 | ATATCGTAAGCAGTA[A/G]GCATTCACATCTCCA | 63893 |
| rs143436337 | snp | A/G | 0.0115144 | 0.0749975 | intron-variant | UBE2O | GRCh38.p7 | 17:76401605 | CTAATACTGCCGGGC[A/G]CGGTGGCTCACGCCT | 63893 |
| rs143447739 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76416066 | GTACATACACGTATA[C/T]ACGTATGTGTATACA | 63893 |
| rs143482331 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | UBE2O | GRCh38.p7 | 17:76431711 | AGCTGGGAAGCCCAG[C/T]GGGGGGGACTGCTTG | 63893 |
| rs143544280 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76416102 | ACATACATGTATATG[C/T]GTATGTGTATACATA | 63893 |
| rs143562804 | snp | C/T | 0.00676609 | 0.0577691 | intron-variant | UBE2O | GRCh38.p7 | 17:76438043 | CCACACTGCTATTAC[C/T]GGCAGGACCAGCCAC | 63893 |
| rs143603390 | snp | C/G | 0.0174175 | 0.0916809 | intron-variant | UBE2O | GRCh38.p7 | 17:76406660 | CCAACCAGCAGTGCA[C/G]AGAGTCCCATGGGAA | 63893 |
| rs143631216 | in-del | -/AAAT/AAATAAAT | | | intron-variant | UBE2O | GRCh38.p7 | 17:76423693 | GGACACTCCATCTCA[-/AAAT/AAATAAAT]AAATAAATAAATAAA | 63893 |
| rs143636767 | in-del | -/TGTGTTTTTGAC | 0.0905309 | 0.192535 | intron-variant | UBE2O | GRCh38.p7 | 17:76446898 | TCTCTAGAAATGCAA[-/TGTGTTTTTGAC]AGTTATTTTGAGAAT | 63893 |
| rs143645638 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBE2O | GRCh38.p7 | 17:76402946 | GCTGCCTGGAGGGAA[C/T]GGGGTGGGTGATGCA | 63893 |
| rs143686201 | snp | C/T | 0.000527122 | 0.016226 | missense | UBE2O | GRCh38.p7 | 17:76396328 | TCTACAATGGCCACA[C/T]TGTCCAGGGTCTTCT | 63893 |
| rs143709633 | snp | C/T | 6.60415e-05 | 0.00574599 | missense | UBE2O | GRCh38.p7 | 17:76405520 | GGACTCACGGTGGAT[C/T]GCATGTGCCGGACCA | 63893 |
| rs143736746 | snp | A/C | 1.74634e-05 | 0.0029549 | intron-variant | UBE2O | GRCh38.p7 | 17:76398624 | GACTAGCTAAGGGAT[A/C]CCGGCTAAGGAGCCC | 63893 |
| rs143803675 | snp | C/T | 0.0107246 | 0.0724382 | intron-variant | UBE2O | GRCh38.p7 | 17:76426287 | ATTACAGGCGTGAAC[C/T]ACCATGCCCAGCCAA | 63893 |
| rs143848002 | snp | A/G | 0.0150606 | 0.0854603 | intron-variant | UBE2O | GRCh38.p7 | 17:76416206 | TATGTGTATATGTGT[A/G]TGTATATGTATGTAT | 63893 |
| rs143864853 | snp | C/T | 0.0126979 | 0.078662 | intron-variant | UBE2O | GRCh38.p7 | 17:76435190 | ATCCAAAGCTCTGAC[C/T]TGCCAAATACAGAGC | 63893 |
| rs143944165 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76393305 | GAGTATAGCTCTGTC[A/C]CCAGGCTGGAGTGCA | 63893 |
| rs144021453 | in-del | -/C | 0.00636936 | 0.0560724 | intron-variant | UBE2O | GRCh38.p7 | 17:76411221 | GGTTTTGCCATGTTA[-/C]CCAGGCTGGTCTCAA | 63893 |
| rs144076918 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE2O | GRCh38.p7 | 17:76434175 | AATAAGGGGCTCCAG[C/T]GAAATGACCCCGAGG | 63893 |
| rs144131784 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76454891 | CAGCACTTTGGGAGA[C/T]CGAGGCGGGTGGGAG | 63893 |
| rs144152682 | snp | C/T | 0.000132336 | 0.00813331 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76391162 | GTCTGGTGCGGTCTC[C/T]GAAGTCTGGTCTGTG | 63893 |
| rs144213637 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76403298 | TTTTAGAGACAGGGT[C/G]TTGCTCTATTGCCCA | 63893 |
| rs144233011 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE2O | GRCh38.p7 | 17:76450276 | AGGTCCCAGGACCCA[C/T]CCTACCACCCTGCTT | 63893 |
| rs144463158 | snp | C/T | 0.00513623 | 0.0504156 | intron-variant | UBE2O | GRCh38.p7 | 17:76398794 | CAACCCGGGCCCTCA[C/T]TGGCGACCACCCTGC | 63893 |
| rs144543657 | snp | A/C/G | 0.00046358 | 0.0152178 | missense, synonymous-codon | UBE2O | GRCh38.p7 | 17:76405293 | GTCGATGTTGACGTC[A/C/G]ATCACCGTGCCACAC | 63893 |
| rs144556802 | snp | A/G | 0.00132148 | 0.0256709 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76391147 | GGGTGGCACCGATGC[A/G]TCTGGTGCGGTCTCC | 63893 |
| rs144558559 | snp | G/T | 0.0182019 | 0.0936463 | intron-variant | UBE2O | GRCh38.p7 | 17:76429003 | GCCTCCTGGGTTCAA[G/T]CAATTCTCCTGCCTC | 63893 |
| rs144647456 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76405260 | GATGCAGTTGGTGCC[A/G]ATGAGCTTGACGGCA | 63893 |
| rs144685854 | snp | A/G | 0.178785 | 0.239642 | intron-variant | UBE2O | GRCh38.p7 | 17:76429091 | ATTTTTAGTAGAGAC[A/G]GGGTTTAACCATGTT | 63893 |
| rs144767720 | snp | G/T | 0.029116 | 0.117091 | intron-variant | UBE2O | GRCh38.p7 | 17:76409473 | ACGACCTCAGCTCAC[G/T]GCAACCTCCGCCTCT | 63893 |
| rs144781075 | snp | G/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76417075 | TCTCTGGGCACCAGA[G/T]GCCTCATCAGGGGGT | 63893 |
| rs144807330 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76444476 | CAGGAGGCGGAGGCT[A/G]CAGTAAGGTGTGATC | 63893 |
| rs144808404 | snp | A/C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76448665 | AAGCTAAAGCATAAA[A/C/T]GCTTTGCCTCCGAAA | 63893 |
| rs144887234 | snp | C/T | 0.00755907 | 0.0610114 | intron-variant | UBE2O | GRCh38.p7 | 17:76414710 | GAGTCCAACTGCCTG[C/T]TAAGTGAGGGGGAAG | 63893 |
| rs144957338 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE2O | GRCh38.p7 | 17:76447288 | TCAGATTCCTCCACT[C/T]AGAAGTGTGACACTG | 63893 |
| rs144974379 | snp | G/T | 0.00716266 | 0.059414 | intron-variant | UBE2O | GRCh38.p7 | 17:76446511 | AACAGGGATAAAAGT[G/T]AAGTAGAGATGGGGA | 63893 |
| rs144974784 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76421199 | AGCTACAGTGAGCTC[C/T]CTAGAGCTGAGCCCA | 63893 |
| rs145098939 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76447281 | TTTGTATTCAGATTC[C/T]TCCACTTAGAAGTGT | 63893 |
| rs145105650 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76426761 | TGGTTTTTAATCCTC[C/T]CCAAATTAGTGACGA | 63893 |
| rs145151094 | snp | C/T | 0.0111196 | 0.0737302 | downstream-variant-500B | UBE2O | GRCh38.p7 | 17:76389227 | TGAGGGGCACACCAC[C/T]GGCCAGGAGGAGGCC | 63893 |
| rs145165800 | snp | C/T | 0.021333 | 0.101051 | intron-variant | UBE2O | GRCh38.p7 | 17:76431440 | AGAATTGCTTGAATC[C/T]GGGAGGCACAGGTTG | 63893 |
| rs145213697 | snp | A/C | 0.0107246 | 0.0724382 | intron-variant | UBE2O | GRCh38.p7 | 17:76403587 | ACTCTGCCTGAACTC[A/C]TATATTTTAATATAC | 63893 |
| rs145217622 | snp | A/T | 0.00636936 | 0.0560724 | intron-variant | UBE2O | GRCh38.p7 | 17:76430614 | TGATCAATCAAAGTG[A/T]TATCTGTCAAAGCAA | 63893 |
| rs145272323 | snp | C/T | 0.000164745 | 0.00907442 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76402640 | GATGATCTGGTTCTT[C/T]AAGTCGTAGACCTTC | 63893 |
| rs145318526 | snp | A/G | 0.02016 | 0.0983543 | intron-variant | UBE2O | GRCh38.p7 | 17:76392846 | CAGTCCCAGCTACTC[A/G]GGAGGCTGAGGTGGG | 63893 |
| rs145419133 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76443981 | ATCCCAGCACTTTGG[A/G]AAGCTGAGGCGGATG | 63893 |
| rs145489220 | snp | A/G | | | synonymous-codon | UBE2O | GRCh38.p7 | 17:76402094 | CGGGCAGACGTCGTA[A/G]AGCTTGGCGCCATCT | 63893 |
| rs145520691 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UBE2O | GRCh38.p7 | 17:76413228 | GTGGAGGAAGTAAGG[A/G]CCAGTGACATTCACC | 63893 |
| rs145528320 | snp | C/G | 0.00318978 | 0.0398085 | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76452039 | CTGGATTATTTTTTT[C/G]AAGGAGTCCATATGC | 63893 |
| rs145532674 | snp | C/T | 0.0240643 | 0.107019 | intron-variant | UBE2O | GRCh38.p7 | 17:76408245 | GAACCGACGTGCTCC[C/T]GGCGAATGCAAGAGC | 63893 |
| rs145563760 | snp | C/G | 0.0166325 | 0.0896639 | intron-variant | UBE2O | GRCh38.p7 | 17:76448239 | AATCACAGAACAGCT[C/G]TTAAGAGTCTACAAG | 63893 |
| rs145605062 | snp | A/C/G | 0.0117499 | 0.0757434 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76396585 | CACAGCCCCCTGGAC[A/C/G]GCAGCTGTGGCTGCC | 63893 |
| rs145686891 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76425751 | TTTGTCAAATACCTA[A/T]CCATAACTTTTCTAA | 63893 |
| rs145702295 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76411154 | ATAGCTGGGACTACA[C/G]GCGTACGCCACCATG | 63893 |
| rs145776892 | snp | A/G | 0.00239616 | 0.0345303 | | | GRCh38.p7 | 17:76390540 | GGAATTGTTGGCGCA[A/G]CCCACACTTCATGCA | 63893 |
| rs145875708 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76407650 | CCTGTTCAGCCTAAC[A/G]GCACCCTTGGGAGTG | 63893 |
| rs145920020 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76394594 | ACAAATCATACAAAA[C/T]ATTATGTACTTATGG | 63893 |
| rs145974683 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | UBE2O | GRCh38.p7 | 17:76418263 | CACAGCCTCCCGGAG[A/G]GCTCTCCAGGCCTCA | 63893 |
| rs146095286 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | UBE2O | GRCh38.p7 | 17:76437925 | AAGATGGGGGACAGG[C/G]TAAATACACGCTTCG | 63893 |
| rs146132298 | snp | A/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76423725 | AAATAAATAAATAAA[A/T]AAAAAATAAGGTCAG | 63893 |
| rs146250821 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76442632 | AAGGGAACGGCACAA[C/T]TGAGTTGGGGAAAAG | 63893 |
| rs146300547 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE2O | GRCh38.p7 | 17:76443488 | GAGATGGGGTTTCAC[C/T]ATGTTGGCCAGGCTG | 63893 |
| rs146323950 | snp | G/T | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76406920 | GGCCAGGCTGGTCTC[G/T]AACTCCTGACCTCGT | 63893 |
| rs146335482 | snp | C/T | 0.0142736 | 0.0832652 | intron-variant | UBE2O | GRCh38.p7 | 17:76445887 | TCCGAACGGGCACTC[C/T]TGCTCAGTAAGAGCT | 63893 |
| rs146335630 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE2O | GRCh38.p7 | 17:76402947 | CTGCCTGGAGGGAAC[A/G]GGGTGGGTGATGCAG | 63893 |
| rs146338254 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76422538 | GAAACATCTGGAACA[C/T]GAGACAGTCCTGCAG | 63893 |
| rs146368524 | in-del | -/A | 0.00914312 | 0.0669923 | intron-variant | UBE2O | GRCh38.p7 | 17:76449220 | CTCCAATTTACAGAG[-/A]AAAACTACAAAAATA | 63893 |
| rs146409025 | snp | C/T | 0.0123036 | 0.0774623 | intron-variant | UBE2O | GRCh38.p7 | 17:76416008 | ACGTATATACGTATG[C/T]GTATACATATGTACA | 63893 |
| rs146433330 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76413773 | AAACATGCAAACCAA[C/G]ACAAAACCCAAGACC | 63893 |
| rs146627981 | in-del | -/ACA | 0.178785 | 0.239642 | intron-variant | UBE2O | GRCh38.p7 | 17:76433184 | AAAGGTGAAAATGAC[-/ACA]ACAACAAATGTCCAT | 63893 |
| rs146639833 | snp | A/G | 5.00221e-05 | 0.00500085 | intron-variant | UBE2O | GRCh38.p7 | 17:76399000 | TGCCACCCTGCGGGT[A/G]CAGGCCAGTCAGCAG | 63893 |
| rs146655478 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76425748 | ACTTTTGTCAAATAC[C/T]TATCCATAACTTTTC | 63893 |
| rs146676702 | snp | C/G | 0.00318978 | 0.0398085 | intron-variant | UBE2O | GRCh38.p7 | 17:76420005 | GCGAATGCACAGAAG[C/G]ATGACATAACCTTGG | 63893 |
| rs146763656 | snp | A/C | 0.0126979 | 0.078662 | intron-variant | UBE2O | GRCh38.p7 | 17:76416068 | ACATACACGTATATA[A/C]GTATGTGTATACATA | 63893 |
| rs146785369 | snp | A/T | 0.0107246 | 0.0724382 | intron-variant | UBE2O | GRCh38.p7 | 17:76398726 | AGGGCAGTCCCCTTC[A/T]GGACCTCATTTTAGC | 63893 |
| rs146796302 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE2O | GRCh38.p7 | 17:76394365 | GGGCTTGCCTGTTCC[A/G]GAAGGATGCACTCAG | 63893 |
| rs146796544 | snp | C/G | 0.00716266 | 0.059414 | intron-variant | UBE2O | GRCh38.p7 | 17:76438877 | CATGCATGCATAGGT[C/G]ACGCCATGCACACCG | 63893 |
| rs146884134 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE2O | GRCh38.p7 | 17:76435509 | CAGACAAGCTAATTC[A/G]CAATATTCCCCCCGT | 63893 |
| rs146938642 | snp | A/G | 0.0126979 | 0.078662 | intron-variant | UBE2O | GRCh38.p7 | 17:76436196 | AGGTTACAGTGAGCC[A/G]AGATAGCACCATTGC | 63893 |
| rs146958741 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE2O | GRCh38.p7 | 17:76444720 | TTCCCCCAGTACAGT[A/G]CTGGGATGACCCAAA | 63893 |
| rs146958824 | snp | A/G | 0.000818452 | 0.0202128 | intron-variant | UBE2O | GRCh38.p7 | 17:76401192 | AAAGTCCCCGTGAGC[A/G]GTGTCTCCATGGGTG | 63893 |
| rs147052788 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE2O | GRCh38.p7 | 17:76421351 | AGCATGGAACATAAT[C/T]TGAGTGACTATTTTC | 63893 |
| rs147062349 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76416137 | CATATATGTGCGTGT[A/G]TAGATATATAAAGTG | 63893 |
| rs147116338 | snp | C/G | 1.65168e-05 | 0.00287369 | missense | UBE2O | GRCh38.p7 | 17:76391479 | GGGGCCGCCGCACCA[C/G]CTGGGTCATGGACTG | 63893 |
| rs147212136 | snp | A/G | 0.0166325 | 0.0896639 | intron-variant | UBE2O | GRCh38.p7 | 17:76401831 | CAGTGAGCCGAGATC[A/G]CACCGTTGCACTCCA | 63893 |
| rs147222155 | snp | C/T | 1.64762e-05 | 0.00287016 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76396351 | GGTCTTCTTGAGGTT[C/T]TCCTGTAGCTTCTTG | 63893 |
| rs147297798 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76411925 | TGAGCTCAAGTGATC[C/T]TCTTGCCTCAGCCTC | 63893 |
| rs147318124 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76416252 | TATGTGTGTATATGT[A/G]TGTATATGTATATAT | 63893 |
| rs147327848 | snp | A/G | 0.0185938 | 0.0946107 | intron-variant | UBE2O | GRCh38.p7 | 17:76415941 | CGTATATACGTATGC[A/G]TATACATATGCACAT | 63893 |
| rs147349982 | snp | C/G/T | 0.00163019 | 0.0285037 | missense | UBE2O | GRCh38.p7 | 17:76396284 | CCTCCTTGCGCTCTA[C/G/T]GTCGGGCACTGCTTC | 63893 |
| rs147427574 | in-del | -/GCCCAAG | 0.0279526 | 0.114869 | intron-variant | UBE2O | GRCh38.p7 | 17:76429872 | CCTGCCCCTTGCTCT[-/GCCCAAG]GTACCTCAATCTGGT | 63893 |
| rs147456701 | snp | C/T | 4.94214e-05 | 0.00497074 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76399547 | GCTCTTTTTGCGACT[C/T]GTGCCGCTGCCGCTC | 63893 |
| rs147497740 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76446682 | GATGACAGCAGCAGA[A/G]CGGACAGGAGGTCAA | 63893 |
| rs147699050 | snp | A/C | 0.0329836 | 0.124112 | intron-variant | UBE2O | GRCh38.p7 | 17:76421392 | TTTTTTTTGAGACGG[A/C]GTTTCGCTCTTGTTG | 63893 |
| rs147713864 | snp | A/G | 3.37007e-05 | 0.00410478 | missense | UBE2O | GRCh38.p7 | 17:76396631 | ACTCCCTTGTCCTCA[A/G]GGGCCACCGGCTGCT | 63893 |
| rs147727800 | snp | A/G | 0.0189856 | 0.0955633 | intron-variant | UBE2O | GRCh38.p7 | 17:76408279 | GGAGTTTTTCGCCTC[A/G]TGCTAACCAGGTGCT | 63893 |
| rs147792246 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBE2O | GRCh38.p7 | 17:76441286 | TACTCAAAACAACTA[C/T]CATATTTACATCCTA | 63893 |
| rs147892337 | snp | C/G | 3.29527e-05 | 0.00405898 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76396345 | GTCCAGGGTCTTCTT[C/G]AGGTTTTCCTGTAGC | 63893 |
| rs147935488 | snp | C/T | 0.000181817 | 0.00953285 | missense | UBE2O | GRCh38.p7 | 17:76391472 | ACCTCGGGGGGCCGC[C/T]GCACCAGCTGGGTCA | 63893 |
| rs147941270 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBE2O | GRCh38.p7 | 17:76444493 | AGTAAGGTGTGATCA[C/T]GCCACTGCATTCCAG | 63893 |
| rs148045392 | snp | A/G | 0.0182134 | 0.0936748 | intron-variant | UBE2O | GRCh38.p7 | 17:76416103 | CATACATGTATATGC[A/G]TATGTGTATACATAT | 63893 |
| rs148073031 | snp | C/T | 9.76563e-05 | 0.00698703 | missense | UBE2O | GRCh38.p7 | 17:76405316 | TGCCACACTGACTGT[C/T]CTGGGGGAGGGGAGG | 63893 |
| rs148077751 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE2O | GRCh38.p7 | 17:76445898 | ACTCTTGCTCAGTAA[A/G]AGCTGCAAATGTGGA | 63893 |
| rs148184667 | snp | C/T | 7.39987e-05 | 0.00608226 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76391988 | CAGGCGGCCACTGCA[C/T]TGGGAGAGGTAGCAG | 63893 |
| rs148214694 | snp | C/G | 0.000172063 | 0.00927371 | intron-variant | UBE2O | GRCh38.p7 | 17:76396015 | ATGGTTTGCCCTGGG[C/G]CAGTAGCTGGGGTCT | 63893 |
| rs148266660 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE2O | GRCh38.p7 | 17:76402207 | TCTGAGATGCCAATG[C/T]GCCCACATGCCCTAA | 63893 |
| rs148300246 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | UBE2O | GRCh38.p7 | 17:76450349 | CCTGTATCTATAGCT[C/G]ATGGTAACAGAGCTA | 63893 |
| rs148309345 | snp | G/T | 0.00597247 | 0.0543191 | intron-variant | UBE2O | GRCh38.p7 | 17:76422813 | AGTCTGTGTGCCCCA[G/T]GGGGGTTAGAATGTG | 63893 |
| rs148402990 | snp | C/T | 0.0908922 | 0.192833 | intron-variant | UBE2O | GRCh38.p7 | 17:76424098 | TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT | 63893 |
| rs148532325 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76434395 | GGAAGGAAACCCCAA[C/T]GCGTAGGAAACACAG | 63893 |
| rs148560915 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBE2O | GRCh38.p7 | 17:76417083 | CACCAGATGCCTCAT[C/T]AGGGGGTTGGGCAAC | 63893 |
| rs148583039 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBE2O | GRCh38.p7 | 17:76440113 | AATCTCAGGTAATGC[C/T]AGGTGCTATGAGGGA | 63893 |
| rs148670541 | in-del | -/G | 0.0134861 | 0.0810011 | downstream-variant-500B | UBE2O | GRCh38.p7 | 17:76389318 | GCAGTGTGGGCGGGT[-/G]GGGGTGCTGTTCACA | 63893 |
| rs148708916 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76410529 | CGCAGGTGCTGAGAC[A/C]CGAACAATGGCAGAG | 63893 |
| rs148709308 | snp | A/G | 0.000757788 | 0.0194504 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76396288 | CTTGCGCTCTACGTC[A/G]GGCACTGCTTCCATC | 63893 |
| rs148739186 | snp | C/G | 0.00199481 | 0.0315187 | intron-variant | UBE2O | GRCh38.p7 | 17:76398032 | ATGTAACCAGCGGCA[C/G]CTCAAGAAGCCTGAC | 63893 |
| rs148795177 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76403804 | CAAAAAGTACAAGAT[A/G]AGCCTGGCACATCTC | 63893 |
| rs148804872 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | UBE2O | GRCh38.p7 | 17:76444082 | AAATATTACTCGGAC[A/G]TGGTGGCGGGAGCCT | 63893 |
| rs148812781 | snp | A/G | 1.65441e-05 | 0.00287607 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76397856 | CTCCACCTTGCTGCT[A/G]ACGTCCACACGGGCC | 63893 |
| rs148816056 | snp | C/G | 0.00517822 | 0.0506191 | intron-variant | UBE2O | GRCh38.p7 | 17:76413385 | GCACTTTTTTTCAAA[C/G]CATGTGTTGTGACCC | 63893 |
| rs148849885 | snp | C/G | 0.00676609 | 0.0577691 | intron-variant | UBE2O | GRCh38.p7 | 17:76400609 | CAGCACTCTCTTTAG[C/G]CAGCTGCCCAAAGCC | 63893 |
| rs148911462 | snp | A/G | 0.00755907 | 0.0610114 | intron-variant | UBE2O | GRCh38.p7 | 17:76445625 | CCAAGGATCCATCCA[A/G]TACAGTCAGCCTGGA | 63893 |
| rs148933113 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBE2O | GRCh38.p7 | 17:76425858 | TCCTGCAGAATTCCA[C/T]CCTGTCTCTCTAACT | 63893 |
| rs149058286 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE2O | GRCh38.p7 | 17:76435820 | CAGACCAGCCTGTCC[C/T]GCAAAGCTCAGTGAC | 63893 |
| rs149066047 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76447589 | GATTCATTCCATCCC[C/T]CTCCTGGAGGACGGC | 63893 |
| rs149087788 | snp | A/C | 0.0279526 | 0.114869 | intron-variant | UBE2O | GRCh38.p7 | 17:76421338 | TTAAAGACACTAGAG[A/C]ATGGAACATAATTTG | 63893 |
| rs149178826 | snp | C/T | 8.31497e-05 | 0.00644732 | missense | UBE2O | GRCh38.p7 | 17:76399854 | TCCATGGAATGGTCC[C/T]GGGAACACTGGGTGT | 63893 |
| rs149193728 | snp | A/C | 4.94849e-05 | 0.00497393 | missense | UBE2O | GRCh38.p7 | 17:76395830 | CTTGGCTTCTGGAGG[A/C]TGGAACTCAATTTTC | 63893 |
| rs149251073 | snp | A/G | 1.71155e-05 | 0.00292531 | intron-variant | UBE2O | GRCh38.p7 | 17:76391891 | TCCTTCTTGGCTGGG[A/G]GCCTGGCCCTATACT | 63893 |
| rs149267279 | snp | C/T | 8.26262e-05 | 0.006427 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76391144 | ACTGGGTGGCACCGA[C/T]GCGTCTGGTGCGGTC | 63893 |
| rs149287414 | snp | C/G | 8.27849e-05 | 0.00643316 | missense | UBE2O | GRCh38.p7 | 17:76405278 | GAGCTTGACGGCACA[C/G]TCGATGTTGACGTCG | 63893 |
| rs149322424 | snp | A/G | 0.0279526 | 0.114869 | intron-variant | UBE2O | GRCh38.p7 | 17:76406220 | ATTGTCTCTTTACGC[A/G]CAGCTGGCAGCGGCC | 63893 |
| rs149387017 | snp | C/G | 0.0221141 | 0.102801 | intron-variant | UBE2O | GRCh38.p7 | 17:76415115 | GTCCTGTGGCTGCCG[C/G]GCATCCCTGAGAACA | 63893 |
| rs149440030 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76416471 | TTTGGGGGAAACAGC[A/G]GTGTTCCCCTGTAGC | 63893 |
| rs149462827 | snp | G/T | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76428641 | TCCATACTGGAAGCT[G/T]TCTGAACATATCCAG | 63893 |
| rs149524848 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76442162 | TCTAGCTAGCTCTAG[C/T]CTAGTCCACAATGCA | 63893 |
| rs149639572 | snp | A/G | 0.000153988 | 0.00877328 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76391501 | CATGGACTGCACCAC[A/G]CGGATCAGCGCCATC | 63893 |
| rs149705708 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76454195 | AAAATATAAAAAGTA[A/G]GCCGGGCGCGGCAGC | 63893 |
| rs149740559 | snp | C/G | 0.000153988 | 0.00877328 | missense | UBE2O | GRCh38.p7 | 17:76396262 | GGTGACTGCCCCTCG[C/G]GCTTGTCCTCCTTGC | 63893 |
| rs149765682 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | UBE2O | GRCh38.p7 | 17:76393525 | GGCGTGAGCCACCAC[A/G]CCCGGCCAACCCTGT | 63893 |
| rs149783036 | snp | A/C/T | 0.000263546 | 0.0114763 | missense | UBE2O | GRCh38.p7 | 17:76399542 | GGGATGCTCTTTTTG[A/C/T]GACTCGTGCCGCTGC | 63893 |
| rs149841558 | snp | A/G | 0.0134861 | 0.0810011 | intron-variant | UBE2O | GRCh38.p7 | 17:76407594 | GGAGGAGAGAAGAAC[A/G]CAGACACAGACCTAA | 63893 |
| rs149925561 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE2O | GRCh38.p7 | 17:76434036 | CCTAACATCTTCTAC[C/T]CTTAGAAATTAGATG | 63893 |
| rs149968933 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76421151 | TTCGCTCCAAAAGGC[C/T]GTTGCTCCTCTGACA | 63893 |
| rs149979963 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | UBE2O | GRCh38.p7 | 17:76429794 | GAGCAGGCAGGGGCA[A/T]GGCTGGGATTTGCTC | 63893 |
| rs150051080 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76443898 | TATAGTCTGGTATAA[C/T]AGAACCCCAAGGAAG | 63893 |
| rs150106987 | snp | C/T | 0.0023933 | 0.0345097 | intron-variant | UBE2O | GRCh38.p7 | 17:76441194 | CACAGCAGGAATCCA[C/T]TGACACTGGCTGGAT | 63893 |
| rs150209609 | snp | A/G | 6.63002e-05 | 0.00575729 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76391462 | CTGCTCAAAGACCTC[A/G]GGGGGCCGCCGCACC | 63893 |
| rs150212378 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBE2O | GRCh38.p7 | 17:76414757 | CTGGCAGGGGGCCAG[C/T]GGGCTGGTCTCTGCA | 63893 |
| rs150241610 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | UBE2O | GRCh38.p7 | 17:76399167 | GGGTTCCAAGGCCAC[A/G]CATTCTCTGAGAACA | 63893 |
| rs150263578 | snp | A/C/G | 0.000132873 | 0.00814997 | missense, synonymous-codon | UBE2O | GRCh38.p7 | 17:76396687 | TATCTTGGGGTGCTC[A/C/G]TCCTCCACCAGCCCA | 63893 |
| rs150442600 | snp | A/G | 0.00597247 | 0.0543191 | downstream-variant-500B | UBE2O | GRCh38.p7 | 17:76389089 | TAGCGTCCAGGAGTT[A/G]TGGCACCTGTCCACC | 63893 |
| rs150451487 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBE2O | GRCh38.p7 | 17:76435615 | AGGTGCTGTGCTGAG[C/T]CCTCTCGAAGGTGAT | 63893 |
| rs150506788 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76433283 | CAAATGAAGTACTGA[C/T]ACATGCTACAACATG | 63893 |
| rs150536678 | snp | C/T | 0.00123648 | 0.0248337 | intron-variant | UBE2O | GRCh38.p7 | 17:76391630 | TGTGTGGGCGGGACA[C/T]CTTCCCTCAGTGGGT | 63893 |
| rs150593082 | in-del | -/CTT | | | intron-variant | UBE2O | GRCh38.p7 | 17:76409401 | AATGAACACACACTA[-/CTT]TTTTTTTTTTTGAGA | 63893 |
| rs150608519 | in-del | -/A | | | intron-variant | UBE2O | GRCh38.p7 | 17:76434795 | TTTTTTTTTTTTTTT[-/A]AAAAAAACAAACAAA | 63893 |
| rs150614225 | snp | C/T | 0.0185938 | 0.0946107 | intron-variant | UBE2O | GRCh38.p7 | 17:76407265 | GAAAGGTCAGGCTCT[C/T]CTTATCTCTGCTCCA | 63893 |
| rs150675311 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76452231 | TAATGCAGCCTGTAA[A/G]CTAGTGAACTTCTTG | 63893 |
| rs150733080 | snp | A/G | 0.000220231 | 0.0104913 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76392018 | GAAGTGGGGGGGCAC[A/G]GCTGGGTAGATGTTG | 63893 |
| rs150740918 | in-del | -/GGGT | | | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76451778 | GTGTGAGATACAGGG[-/GGGT]GTGTGTGTGTGTGTG | 63893 |
| rs150746827 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76428173 | ATGAGGTTGAAAAAT[C/G]CAATCCATCTTCATT | 63893 |
| rs150768445 | snp | C/G | 0.0225045 | 0.103662 | intron-variant | UBE2O | GRCh38.p7 | 17:76402804 | ATGGGGGAGGATCTA[C/G]ACAGCTCACTGACTG | 63893 |
| rs150786122 | snp | C/T | 1.64982e-05 | 0.00287208 | missense | UBE2O | GRCh38.p7 | 17:76398951 | CATCCTGCCACATCA[C/T]GTCGGCTGAGGTCAT | 63893 |
| rs150827099 | in-del | -/T | 0.0115144 | 0.0749975 | intron-variant | UBE2O | GRCh38.p7 | 17:76392350 | CTGTGTCCCCCAGGC[-/T]TGGAGTACACTAGTG | 63893 |
| rs150832597 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE2O | GRCh38.p7 | 17:76410700 | CCGAAGCTATGCTGG[A/G]GGCCACTCAGAGCAG | 63893 |
| rs150885501 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76415974 | ACGTATATACGTATG[C/T]GTATACATATGCACA | 63893 |
| rs150921393 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | UBE2O | GRCh38.p7 | 17:76444857 | TGAATACCGGGATGC[A/T]TTCAGCACTGCATAT | 63893 |
| rs150981902 | in-del | -/TA | 0.0279526 | 0.114869 | intron-variant | UBE2O | GRCh38.p7 | 17:76416030 | ATATGTACACACACG[-/TA]TATATGTGTGTGTAC | 63893 |
| rs151024961 | snp | A/T | 0.00438332 | 0.0466095 | intron-variant | UBE2O | GRCh38.p7 | 17:76434561 | AATTAGGGTGACTCC[A/T]CGTCCTGGGGAAAGG | 63893 |
| rs151029911 | snp | A/G | 0.0128111 | 0.0790026 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76391342 | GGCCTTGGGCACCCC[A/G]TTGGGCAGTGCCTGG | 63893 |
| rs151077191 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBE2O | GRCh38.p7 | 17:76440754 | TTTCTTAAAATTTTA[C/T]TGGAACATGACCATG | 63893 |
| rs151153378 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76447982 | ATCATATCGGGGTTA[A/G]GAAGATAGACCTCTT | 63893 |
| rs151207723 | snp | C/T | 0.0103295 | 0.0711199 | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76455180 | CCTGAAATCCCAACA[C/T]TTTGACTGCGCCTGA | 63893 |
| rs151288373 | snp | C/G | 0.00279162 | 0.0372561 | intron-variant | UBE2O | GRCh38.p7 | 17:76404135 | CAATGGCTGGCGCAG[C/G]GGGAACTGTGAATGG | 63893 |
| rs151336177 | snp | A/G | 1.68906e-05 | 0.00290603 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76399877 | CTGGGTGTCTGGGGA[A/G]CATGACATGATCCGC | 63893 |
| rs180677320 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE2O | GRCh38.p7 | 17:76417216 | GACTCAGGGGCAGGC[C/T]TCTGCTCTTCACATG | 63893 |
| rs180691509 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76436949 | CCAGCCTGGCCAACA[C/T]GTTGAAACCATTTCT | 63893 |
| rs180707982 | snp | C/T | 0.0039913 | 0.044494 | intron-variant | UBE2O | GRCh38.p7 | 17:76405477 | CTAAGGTGGCTGCCC[C/T]CAGGCCCGGGGCTGG | 63893 |
| rs180710439 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant | UBE2O | GRCh38.p7 | 17:76394906 | TTTGAGATGAAGTCT[C/T]GCTCTGTTGCCCAGG | 63893 |
| rs180719941 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76444671 | ATGACTGAAGGCGAG[A/C]GCAGGTCATGAGGAA | 63893 |
| rs180721767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76425936 | CCTGGGAAAAGTCCC[C/T]GGTTTTGGTGAAGAA | 63893 |
| rs180953077 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76399067 | AGAGTCTTTCTGTCC[C/T]TTCCTGTCCCTGTGG | 63893 |
| rs180959205 | snp | A/C | 0.00199481 | 0.0315187 | intron-variant | UBE2O | GRCh38.p7 | 17:76422110 | ACCTCTATGTGTGAT[A/C]AGTAATGGGACGTGT | 63893 |
| rs181137305 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76446059 | CTGGAAAGCACATTA[C/T]AGACGTTCCTGATTG | 63893 |
| rs181276177 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76408815 | AACCTTGGAATAAAC[C/G]CAATCCCTACTGTTA | 63893 |
| rs181291770 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76430545 | TGAAGGGCCACAGTA[C/T]AGAGCTCATGAATCA | 63893 |
| rs181333476 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76428690 | CCTATTTAAAAGTGA[A/G]GCAATAAGAGATCTT | 63893 |
| rs181345164 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76450479 | CCTTGGAATTTCTGC[A/G]TCCCTTGGCTTTTGC | 63893 |
| rs181356161 | snp | C/T | 0.00290512 | 0.0380016 | intron-variant | UBE2O | GRCh38.p7 | 17:76399962 | GGGCTGTGAGGTGCA[C/T]CTGGGCAGGCCTGGC | 63893 |
| rs181459039 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76440255 | TAGTACTTATCATAT[A/G]AGTTATATGTTGATA | 63893 |
| rs181466331 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76421743 | ACTGGTAACTGATGC[A/C]TTGGGACTGCTGGCT | 63893 |
| rs181467946 | snp | A/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76422742 | GAATTGCTCCTCCTC[A/T]TTCTCTATCCACCTG | 63893 |
| rs181469503 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76451310 | ACAAGCATTCTGTTG[C/T]ACAAAAGTAATATTT | 63893 |
| rs181496075 | snp | C/T | 0.0433465 | 0.140692 | intron-variant | UBE2O | GRCh38.p7 | 17:76409113 | AGCTGGGACTACAGG[C/T]GCCCGCCACCACGCC | 63893 |
| rs181558256 | snp | G/T | 0.0103295 | 0.0711199 | intron-variant | UBE2O | GRCh38.p7 | 17:76398695 | CCCGTCTTGGAAGTG[G/T]TGAGACCCCTTCATG | 63893 |
| rs181592417 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76426405 | GTCTGAGTACCTGTC[C/T]TAACTGGCACATATA | 63893 |
| rs181595035 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UBE2O | GRCh38.p7 | 17:76441094 | CTTTCTCTGGGTTTC[A/G]GTCTTTCCTTTTCTA | 63893 |
| rs181597918 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76406026 | GGGAGAAGCAGGACA[A/C]TGGGCTGCGGTGGGT | 63893 |
| rs181611114 | snp | C/T | 0.00358779 | 0.0422022 | intron-variant | UBE2O | GRCh38.p7 | 17:76431186 | TGCAAAGTACTTATA[C/T]ACAACTAGATCTGAA | 63893 |
| rs181797783 | snp | C/G | 0.00795532 | 0.062565 | intron-variant | UBE2O | GRCh38.p7 | 17:76393498 | TTGGCCTCCCAAAGT[C/G]CTGGGATTACAGGCG | 63893 |
| rs181884586 | snp | A/G | 0.00199481 | 0.0315187 | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76451412 | TCTGAGGGGAAGCAG[A/G]GTCCTGTGTGTGGAT | 63893 |
| rs182001457 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE2O | GRCh38.p7 | 17:76393887 | GGCGAGGGAACCTCT[A/G]CACATGCTCTTATCG | 63893 |
| rs182053034 | snp | C/T | 0.0115144 | 0.0749975 | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76454345 | AAAAAAATAGCTGGG[C/T]GTGGTGGCACATGGC | 63893 |
| rs182063878 | snp | C/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76436121 | GCATGGTGGTGTGCA[C/G]CTGTAATCCCAGCTA | 63893 |
| rs182070346 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76415975 | CGTATATACGTATGC[A/G]TATACATATGCACAT | 63893 |
| rs182080788 | snp | A/G | 0.00398564 | 0.0444627 | intron-variant | UBE2O | GRCh38.p7 | 17:76416182 | CATACGTGTGTGTGT[A/G]TATATGTATATGTGT | 63893 |
| rs182089470 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76455020 | TAATCCCAGCTACTC[A/G]GAAGGCTGAGGCAGG | 63893 |
| rs182099976 | snp | G/T | 0.0023933 | 0.0345097 | intron-variant | UBE2O | GRCh38.p7 | 17:76406915 | ATGTTGGCCAGGCTG[G/T]TCTCGAACTCCTGAC | 63893 |
| rs182160701 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76427888 | TTCTGTTTCAACTCC[A/T]TGCTTCACGTGTTCA | 63893 |
| rs182349383 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76410459 | TCAACGAAGAATGGC[A/G]TGGCCAACGCACCCG | 63893 |
| rs182466227 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76447785 | CCCACAACCCGCCTC[A/G]TGCACCTTTTGCTTC | 63893 |
| rs182501227 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76404757 | AAATGTTTTGGGAAG[A/C]AAAAAGACCGGAGGG | 63893 |
| rs182585882 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76429279 | GGGGATGGTGGCTCA[C/G/T]GCCTGTGATCCCAGC | 63893 |
| rs182596935 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76407598 | GAGAGAAGAACGCAG[A/T]CACAGACCTAAATCA | 63893 |
| rs182603369 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76448874 | TGGTGATGGGGAAGG[A/G]GCAAGCCTCCTCTAA | 63893 |
| rs182727441 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76422893 | GGAACACAGAAGGGT[A/G]CCTCTGAGGAGTCAC | 63893 |
| rs182728614 | snp | A/C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76401468 | GCACCCCCTGTATAT[A/C/T]TACTTGTTTGCTGTG | 63893 |
| rs182784601 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76442049 | ATTCAGGAAACCCAC[A/G]TGTGTGGAATCTGCC | 63893 |
| rs182809839 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76433246 | TCTATCCATATGATA[A/G]AATATTATTCAACAA | 63893 |
| rs182821041 | snp | C/T | | | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76452008 | CCAAATTGGTGACTC[C/T]CCTCTACCCAGGGTT | 63893 |
| rs182922939 | snp | C/T | 0.00953873 | 0.0683987 | intron-variant | UBE2O | GRCh38.p7 | 17:76395382 | TTTTTTTAGTGGAGA[C/T]GGGGTTTCACTGTGT | 63893 |
| rs182924623 | snp | C/G/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76437700 | CTTGGATTACAGGCA[C/G/T]GTGCCACTGTGCCTG | 63893 |
| rs183195594 | snp | A/G | 0.00517822 | 0.0506191 | intron-variant | UBE2O | GRCh38.p7 | 17:76418562 | GGTCCCTTGGAAGGA[A/G]GAACAGGTTTTTTTT | 63893 |
| rs183210459 | snp | G/T | 0.00119737 | 0.0244387 | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390860 | GGACAGAGGGGCATG[G/T]GAAGAGGGGTGATTC | 63893 |
| rs183298130 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76442960 | AGAACTGATGACAAG[C/T]TAGAATGAGGGCCAA | 63893 |
| rs183298190 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76452204 | ACAAAAAGAGGCTGG[A/G]TGGCTTCACCATAAT | 63893 |
| rs183312783 | snp | A/T | 0.0023933 | 0.0345097 | intron-variant | UBE2O | GRCh38.p7 | 17:76432292 | AGTATGTTCCTGTCA[A/T]TCCACAAATATTTCA | 63893 |
| rs183313111 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76412030 | TAGTCTCAAACAGAA[A/G]AGGTCCAGCATCATG | 63893 |
| rs183426950 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76411718 | TGAGACAGGGTCTCA[C/T]TCTGCCACCCAGGTT | 63893 |
| rs183427690 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBE2O | GRCh38.p7 | 17:76438760 | TGTTTCCTCTTGCAC[C/T]GGAACAGATCACTGC | 63893 |
| rs183432141 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE2O | GRCh38.p7 | 17:76397251 | GACATATCCTGCTGC[A/G]TTCCCTGGAATGGCC | 63893 |
| rs183432436 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBE2O | GRCh38.p7 | 17:76418858 | ACAGGCGTGAGCCAC[C/T]GCGCCTGTCCGGAAC | 63893 |
| rs183473659 | snp | A/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76392582 | CCTTGCCTGGAATCA[A/T]TGAACCCTGGCTAAG | 63893 |
| rs183512008 | snp | G/T | 0.00318978 | 0.0398085 | intron-variant | UBE2O | GRCh38.p7 | 17:76430316 | ATGTTCAATCTACCA[G/T]GTTTACCTAAAGTAT | 63893 |
| rs183514798 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76408249 | CGACGTGCTCCTGGC[A/G]AATGCAAGAGCTCTG | 63893 |
| rs183564729 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76433480 | GAGGTTTCTTTTTAG[C/G]GTGATGAAAATGTTC | 63893 |
| rs183739586 | snp | A/G | 0.00279162 | 0.0372561 | intron-variant | UBE2O | GRCh38.p7 | 17:76450258 | CTAAGCCACAGTTCT[A/G]CAAGGTCCCAGGACC | 63893 |
| rs183778664 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76442535 | TGCGTGATAGCACAC[A/G]AGCTTTAGGATTTGC | 63893 |
| rs183799207 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76402834 | GGACCGGTTGGCTAC[C/T]AGCCCTAAACAGCTG | 63893 |
| rs183988019 | snp | A/G | 0.0170251 | 0.090679 | utr-variant-5-prime, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76453681 | TAATAGATACGTGTA[A/G]AGCATATGTATAATG | 63893 |
| rs183998108 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE2O | GRCh38.p7 | 17:76424049 | AGTAGCTGGGACTAC[A/G]GGCCCCCGCCACCAT | 63893 |
| rs184063511 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76427236 | CTTCTGCAGATCTGT[G/T]TTCCAGTTCCCATAG | 63893 |
| rs184073835 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76398165 | ACTTTCAGGTCTTGT[C/T]TCCTAGAGCCACCTG | 63893 |
| rs184202535 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76446754 | AGAAATGCCAGTTAC[A/G]TGGAGTGTCTGCACA | 63893 |
| rs184204431 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76420263 | AGGCAGTAAAAATAA[C/T]ACACAAGAGCCCTGA | 63893 |
| rs184208754 | snp | C/T | 0.00517822 | 0.0506191 | intron-variant | UBE2O | GRCh38.p7 | 17:76424199 | AGGCGTGAGCCACCG[C/T]GCCCGGCCTTTTTTT | 63893 |
| rs184229717 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76406284 | AGGCACGTGATGCTC[C/T]CACCAGGCCAGCCTG | 63893 |
| rs184302658 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76439546 | AATAGAATGTATGCC[C/T]AGGCATTCTTGGTTT | 63893 |
| rs184313210 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76403856 | CTTAAAAAACCAACA[A/G]AAAGGGCCATGTGAG | 63893 |
| rs184355285 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76397489 | GTAGGAAAGTCTCCA[C/T]CTCCTTTTAGGAGGG | 63893 |
| rs184395339 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE2O | GRCh38.p7 | 17:76425161 | CAGGCGTGAGCCACC[A/G]CACCCGGTTCACCTG | 63893 |
| rs184426020 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76404299 | ACATGACCAGGGGTA[A/G]AAGTGAACAACCCCA | 63893 |
| rs184624787 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76434171 | ATAAAATAAGGGGCT[C/T]CAGCGAAATGACCCC | 63893 |
| rs184625791 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76392768 | GAGCAGTCTGGCCAA[C/T]GTGGTGAAACCCCGT | 63893 |
| rs184634527 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76414007 | TCCGGCTGGTGCCAG[C/T]GTAAGGACTTTCTCA | 63893 |
| rs184692126 | snp | C/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76452349 | ATGCACAATGCAGTA[C/G]CGAGCTCCTTGGGGG | 63893 |
| rs184740975 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76439889 | CTGCAGGTGGAACTA[A/G]GCTCTCGCTCCCTTA | 63893 |
| rs184782087 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76434937 | AGAGGGGCTCGGGCG[C/T]GCCCATCCAGGGATC | 63893 |
| rs184821998 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76393423 | GTATTTTAATAGAGA[C/T]GGGGTTTCACCATGT | 63893 |
| rs184871867 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76421469 | TTCCCCGGTTCAAGC[G/T]ATTGTCCTGCCTCAG | 63893 |
| rs184921411 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76421829 | TCCCATCCTGGCTGG[A/C]TCTATTTCCCTCAGT | 63893 |
| rs184928905 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76415879 | TACATGTATATACAA[A/G]TATATGTACATACAC | 63893 |
| rs184935795 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76440412 | GGCCCATTGCCACCT[C/T]GACCGCCAGGACTCA | 63893 |
| rs184947149 | snp | A/G | 1.65031e-05 | 0.00287251 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76398952 | ATCCTGCCACATCAC[A/G]TCGGCTGAGGTCATC | 63893 |
| rs185038465 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBE2O | GRCh38.p7 | 17:76416077 | TATATACGTATGTGT[A/G]TACATATGTACATAC | 63893 |
| rs185317799 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76454860 | GGCTGGATGTGGTGG[C/T]TCTTGCCTGTAATCC | 63893 |
| rs185415487 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76435961 | CAAATTCTCATCATC[A/G]TTAGGCCCCGTGCGG | 63893 |
| rs185416511 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76432619 | GGTTAAATCCCAACA[G/T]AATGCAAAATGGCTA | 63893 |
| rs185423054 | snp | C/G | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76411134 | TACTCCCACCTGTCT[C/G]CTGAATAGCTGGGAC | 63893 |
| rs185426664 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76451148 | CTGCAGTCAAATGAG[C/T]TGCGTTCCAAAAATC | 63893 |
| rs185431376 | snp | A/G | 0.00517822 | 0.0506191 | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76451951 | ATACGGGAGTCAGAT[A/G]TCTGCTTAACAGCTT | 63893 |
| rs185436886 | snp | C/G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76441985 | TCCAATAGAGAGCCT[C/G/T]GTTCGTACTTAGCCA | 63893 |
| rs185439132 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76400708 | CCCCAACTGTAACCA[C/T]GGCCCCCACCCAATG | 63893 |
| rs185439439 | snp | A/C | 0.00199481 | 0.0315187 | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76389714 | CCGGCTCCATCCTCC[A/C]GCAGCTCTGCTGGCT | 63893 |
| rs185445013 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76422747 | GCTCCTCCTCATTCT[C/T]TATCCACCTGCTTTA | 63893 |
| rs185459435 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76430593 | ATGCCATATTGACCA[C/T]GAGACTGATCAATCA | 63893 |
| rs185488064 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76426159 | AGATGCACAACACCA[C/T]ACTTGGCTAATTTTT | 63893 |
| rs185546282 | snp | A/G | 0.00914312 | 0.0669923 | intron-variant | UBE2O | GRCh38.p7 | 17:76405130 | AAGAGCACGGAGGAG[A/G]CTGTAGCCCAGAGGT | 63893 |
| rs185548554 | snp | C/G/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76444277 | TGGTCAGCTAGGCAC[C/G/T]GTGGCTCACGTCTGT | 63893 |
| rs185557142 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76445398 | TATTGCTGTGGCCTC[C/T]CTAAAAATGCAAACC | 63893 |
| rs185600073 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76429648 | GAGGACCACATTAGA[C/T]GGAGTAGAAAGCTGG | 63893 |
| rs185663233 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76425324 | TATTTTTTTAAATAA[C/T]AGTTTAGCTTAATTG | 63893 |
| rs185726992 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76449542 | ATCGTGCCACTGCAC[C/T]CCAGCCTGGGTGACA | 63893 |
| rs185729469 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76407975 | GTAACATGGTGGCTA[A/C]ACTCCCTTCCACTGG | 63893 |
| rs185949986 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76393603 | CTTATCCCCAACAAG[A/G]CAAGTAGTACAAGCA | 63893 |
| rs185971683 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76446363 | TGCTGGCCCCCAACA[A/G]GTTCCACTGGATTCC | 63893 |
| rs186002696 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76427122 | TCTCAAGCTGCCTTT[A/C]GGATGCTATTTTTCC | 63893 |
| rs186081659 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76422259 | TGATGTGTGGAAGCA[C/T]GACCTAAATGAACAA | 63893 |
| rs186223642 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE2O | GRCh38.p7 | 17:76399389 | CGCACACCGAGGGGA[C/T]GCGCACTCTGCCTGG | 63893 |
| rs186230075 | snp | A/G | 0.0023933 | 0.0345097 | intron-variant | UBE2O | GRCh38.p7 | 17:76440817 | TTGTGCTATAATGGC[A/G]AAGCTGAGTTGTTGT | 63893 |
| rs186322789 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76442190 | GCACGTAGTCTGCCT[C/G]GGGAGCCCGCGACGG | 63893 |
| rs186328782 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76408838 | TACTGTTAAGGGGTG[C/G]CCTGCTTGTAGTTTA | 63893 |
| rs186360705 | snp | C/T | 0.00318978 | 0.0398085 | intron-variant | UBE2O | GRCh38.p7 | 17:76395282 | CACCTCCCAGGTTCA[C/T]GCCATTCTCCTGCCT | 63893 |
| rs186400397 | snp | A/C | | | intron-variant | UBE2O | GRCh38.p7 | 17:76436140 | TAATCCCAGCTACTC[A/C]GGAGGCTGAGGCAGG | 63893 |
| rs186407665 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76416614 | CACACCAACCTCCCC[A/G]CGCTTCTCAAACACC | 63893 |
| rs186412410 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76455083 | AGTGAGCCTAGATCG[C/T]GCCGCTGCACTCCAG | 63893 |
| rs186426056 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76394597 | AATCATACAAAATAT[C/T]ATGTACTTATGGTGA | 63893 |
| rs186646036 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76417244 | ATGTGGGCACCCCCA[C/T]TGACCATCAGAGCAG | 63893 |
| rs186789571 | snp | C/T | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76452485 | CATGTCTTAGAAGTC[C/T]CCTCAAGTCGGGAAG | 63893 |
| rs186821999 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76434375 | GTCTATGGGAGAAAC[A/G]GAGAGGAAGGAAACC | 63893 |
| rs186989989 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76424685 | TTCAAGACCAGCCTG[A/G]GCAACAGAGTAAGAC | 63893 |
| rs187000616 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE2O | GRCh38.p7 | 17:76442998 | AAATTAAAAATGACC[C/T]CAAATGCTCTAATTT | 63893 |
| rs187003219 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76447296 | CTCCACTTAGAAGTG[C/T]GACACTGGGCAATTT | 63893 |
| rs187008821 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76404002 | TAAGTCCATACTGAT[A/T]AAAAAAAAGAATACA | 63893 |
| rs187100628 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76406195 | GCCCGGCCAACTGCA[C/T]GAGCACCTGATTGTC | 63893 |
| rs187148655 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE2O | GRCh38.p7 | 17:76406360 | GTTCTTCACTGGGTC[A/G]TAATCATGGATGGGT | 63893 |
| rs187218496 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76427440 | TTAGACATTTCTATT[A/G]TAATCTCTTCTATTA | 63893 |
| rs187226581 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76428633 | CTCTACCTTCCATAC[C/T]GGAAGCTTTCTGAAC | 63893 |
| rs187242676 | snp | A/C | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76448555 | ATCACAGACAGCCCT[A/C]ATTTAGAGGCACTAT | 63893 |
| rs187249951 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76406919 | TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTCG | 63893 |
| rs187300387 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76431893 | TTTCAAATGTTAAAG[A/G]AAGTTTAAGTCCCAT | 63893 |
| rs187392074 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76409319 | GTTTCTGAACAGAAA[A/G]AGGACAAGACAAGAT | 63893 |
| rs187544948 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76439754 | CTTCCCGCCCAGGAC[A/G]CCCTGCCCTCCACTG | 63893 |
| rs187546031 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76439122 | CCAGGGGCAGCTGAC[A/G]GCGTGGTTTGGAGGC | 63893 |
| rs187571060 | snp | A/G | 0.000399281 | 0.0141238 | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76451351 | CTTGTAAATGGACTG[A/G]TAATTTTCCTTCCAA | 63893 |
| rs187572069 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE2O | GRCh38.p7 | 17:76419092 | GTTCGAGAACCAGCC[C/T]GGGCAACCTAGTGAG | 63893 |
| rs187573557 | snp | C/T | 0.0228947 | 0.104514 | intron-variant | UBE2O | GRCh38.p7 | 17:76397277 | TGGCCGTTAAGGTGA[C/T]GGGGCAAGCCATTCC | 63893 |
| rs187676156 | snp | A/T | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76449123 | CAGGGAAAGGACATG[A/T]CTTGCTGCCCAGTCT | 63893 |
| rs187690081 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76424125 | ATGTTAGCCAGGATG[A/G]TCTCGATCTCCTGAC | 63893 |
| rs187815986 | snp | A/G | 0.00478085 | 0.0486577 | intron-variant | UBE2O | GRCh38.p7 | 17:76411787 | ACCACCTGGGCTCAA[A/G]TAATCCTTCTGCCTC | 63893 |
| rs187818540 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76392722 | CTTTGGGAGGCCGAG[A/G]CGGGTGGATCACTTA | 63893 |
| rs187822585 | snp | A/C | 0.00874735 | 0.0655527 | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76452091 | GTCGCAGCTGTCAGA[A/C]TCCTCCCCCCCAAGT | 63893 |
| rs187846809 | snp | C/G | 0.00835141 | 0.0640778 | intron-variant | UBE2O | GRCh38.p7 | 17:76423250 | TGGGCACGGTGGTAC[C/G]CACCTGGAGCCCCAG | 63893 |
| rs187852769 | snp | C/T | 6.7473e-05 | 0.00580792 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76402112 | CTTGGCGCCATCTTC[C/T]GTGTTCATGGAGCAC | 63893 |
| rs187971860 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76403686 | CCCAAAAGAGCCAAG[A/T]AGCAATTAGCACACC | 63893 |
| rs188030652 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76397678 | CTGCCTTTCCCCTCA[C/T]GCTTTCGCTGAGATC | 63893 |
| rs188046104 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76442694 | CAGGAGATAGAGCAG[C/G]ATGTGTAGGTGAGGG | 63893 |
| rs188061665 | snp | A/C | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76450283 | AGGACCCACCCTACC[A/C]CCCTGCTTGGTGGTC | 63893 |
| rs188095822 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76430339 | TAAAGTATGCTAACC[A/G]AAGATTTTTTTTTTC | 63893 |
| rs188104021 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76408563 | TCTGGCAGGTCTACA[C/T]ATTTAAAGACAGTGA | 63893 |
| rs188113639 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76433287 | TGAAGTACTGATACA[C/T]GCTACAACATGGATG | 63893 |
| rs188222711 | snp | C/T | 3.3095e-05 | 0.00406773 | synonymous-codon | UBE2O | GRCh38.p7 | 17:76391183 | CTGGTCTGTGTGGTC[C/T]CTGCTAGCTGAGGCC | 63893 |
| rs188326696 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76420637 | TCTTTGCGAGACAAA[C/T]TGGGCTGGGGCGCTG | 63893 |
| rs188342589 | snp | A/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76393057 | TGAGGCCAGGAGGTC[A/T]AAACCAACCTGGGCA | 63893 |
| rs188347932 | snp | G/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76414749 | AGCTTGGCCTGGCAG[G/T]GGGCCAGCGGGCTGG | 63893 |
| rs188411363 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76445828 | CAAGTGGCTCCTGAC[A/G]GAGTCCCCCCGTGGC | 63893 |
| rs188440825 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76426214 | TTGCCATGTTTCCCA[A/G]GCTGGTCTCGAACGG | 63893 |
| rs188446037 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76405969 | TTCTGCCCTCTGCAA[A/G]TGCCTGCCCTAGCTG | 63893 |
| rs188550576 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76429625 | CATAAGCAAGGCTCT[A/G]GACAGGTGAGGACCA | 63893 |
| rs188596613 | snp | C/T | | | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76452244 | AAGCTAGTGAACTTC[C/T]TGGGTTCGGCTGGGA | 63893 |
| rs188777759 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76438002 | GCAATGTGTTCAAAA[C/T]GGAATCTCCCTCCCC | 63893 |
| rs188842381 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76433858 | GAGATGGTGACTCTA[C/T]AAAAAACTTAAAAAG | 63893 |
| rs188847813 | snp | A/G | 0.00716266 | 0.059414 | intron-variant | UBE2O | GRCh38.p7 | 17:76407613 | ACACAGACCTAAATC[A/G]GTGCCGTCACTGATG | 63893 |
| rs188980084 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76435985 | CGTGCGGTGGCTCAC[G/T]CCTGTAATCCTAGCA | 63893 |
| rs189002688 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76393863 | CAGGGAAGGCAGAGC[A/G]CTAGCTGGGGCGAGG | 63893 |
| rs189010469 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76416122 | GTGTATACATATATA[C/T]ATATATGTGCGTGTA | 63893 |
| rs189018767 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76443885 | GAGAAACATTTGGTA[C/T]AGTCTGGTATAATAG | 63893 |
| rs189106573 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76412617 | AAGGGTCTAGCTCCA[C/T]GCTGCCATGTGCCCA | 63893 |
| rs189219809 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76440204 | TGCTACCCAATCCAG[C/T]AGCCACTATGGTAAA | 63893 |
| rs189230867 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76421568 | TGGGGTTTCTCCATG[C/T]TGGTCAGGCTGGTCT | 63893 |
| rs189249478 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76398182 | CCTAGAGCCACCTGG[C/T]GGCAGCATCAGGGAC | 63893 |
| rs189347672 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76425470 | TTAATTTTTTAGCTG[A/T]TTGAATATTTACCTC | 63893 |
| rs189349105 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76421998 | AGGTGGAGGAAAATG[A/G]GAAGATGGAGATGTC | 63893 |
| rs189368363 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76440658 | CAGCTGTGGCTCACA[C/T]TGTATCTCTATTTTT | 63893 |
| rs189389948 | snp | C/T | 0.00398564 | 0.0444627 | intron-variant | UBE2O | GRCh38.p7 | 17:76415940 | ACGTATATACGTATG[C/T]GTATACATATGCACA | 63893 |
| rs189448811 | snp | C/T | 0.00119737 | 0.0244387 | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76453999 | TGCTCATCTGTGAAA[C/T]AGGGATGATAATAGC | 63893 |
| rs189620153 | snp | A/C | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76444593 | AGTGATCAGAAATTC[A/C]CTAGTCATTTGTGAC | 63893 |
| rs189679523 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76393424 | TATTTTAATAGAGAC[A/G]GGGTTTCACCATGTT | 63893 |
| rs189730191 | snp | A/T | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76435267 | AAGGTATACTCACAC[A/T]CATAGAGTTTGGTCA | 63893 |
| rs189753626 | snp | C/T | 0.000798403 | 0.0199641 | utr-variant-3-prime | UBE2O | GRCh38.p7 | 17:76390382 | CAGGCCATGTATAGC[C/T]GGGAGTCAGTGACAG | 63893 |
| rs189826195 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76433244 | GATCTATCCATATGA[C/T]AGAATATTATTCAAC | 63893 |
| rs189832710 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76411628 | GTGCTCTCTTTTAAT[C/T]CCGGGGTAAAAGGCA | 63893 |
| rs189838197 | snp | C/G | | | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76451987 | CAAGAAAAAACCTTC[C/G]GGTTTCCAAATTGGT | 63893 |
| rs189878991 | snp | A/G | 0.0123036 | 0.0774623 | intron-variant | UBE2O | GRCh38.p7 | 17:76406786 | CTCGCTGCAACCTTC[A/G]CCTCCCAGGTTCAAG | 63893 |
| rs189879169 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76417128 | GCTCCAGGCCCTTCC[A/G]GCTACAGCTCCAGAG | 63893 |
| rs189883401 | snp | A/G | 0.0524604 | 0.153226 | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76455122 | ACAGAGTGAGATTCC[A/G]TCTCAAAAAAAAGTA | 63893 |
| rs189893587 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76436471 | AGGATGACTCCAGCA[A/G]TTTTTCTTCGGTGCT | 63893 |
| rs189925694 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE2O | GRCh38.p7 | 17:76404475 | GAAAGGCTGGGAAGC[A/G]ATTCCAGATTGGAGA | 63893 |
| rs190023762 | snp | G/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76430822 | CTTTTGGCCCTTTGG[G/T]CTCACACCACTGATA | 63893 |
| rs190161697 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant, upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76455009 | GCAGCCGCCTGTAAT[C/G]CCAGCTACTCGGAAG | 63893 |
| rs190172179 | snp | A/G | 0.00199481 | 0.0315187 | intron-variant | UBE2O | GRCh38.p7 | 17:76425167 | TGAGCCACCGCACCC[A/G]GTTCACCTGTTTCTT | 63893 |
| rs190207562 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76408010 | TAGAACCCAAGACAA[C/T]GGCATGTGGAAGGAC | 63893 |
| rs190264444 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76451221 | AACTCACAGAAAGAC[A/G]CCAGCAATCATCTGG | 63893 |
| rs190271593 | snp | A/C | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76449577 | GAGACTCTGTTTAAA[A/C]AAGAAACTCACACAC | 63893 |
| rs190393514 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76408868 | AAAAAAAAATTGTTA[C/T]TAGGAGGGGATCTGG | 63893 |
| rs190443746 | snp | C/T | 0.000566148 | 0.0168153 | intron-variant | UBE2O | GRCh38.p7 | 17:76398995 | TCCACTGCCACCCTG[C/T]GGGTGCAGGCCAGTC | 63893 |
| rs190454123 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76429825 | TTTTAGTGTGCAGAC[A/G]TTCATGAATCCCTCT | 63893 |
| rs190488964 | snp | C/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76438380 | AAAGAAAAACTTAAA[C/G]GCTCCTCGTCGCTCT | 63893 |
| rs190499798 | snp | A/G | 0.0103295 | 0.0711199 | intron-variant | UBE2O | GRCh38.p7 | 17:76418821 | TGATCCACCCGCGTC[A/G]GCCTCCCAAAGTGCT | 63893 |
| rs190510373 | snp | C/G | 0.00358779 | 0.0422022 | intron-variant | UBE2O | GRCh38.p7 | 17:76441990 | TAGAGAGCCTCGTTC[C/G]TACTTAGCCATCCTC | 63893 |
| rs190543835 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76401222 | GACCATGCTCTCCAC[A/G]CCTGTGCCCGCTGGC | 63893 |
| rs190544024 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76422817 | TGTGTGCCCCATGGG[A/G]GTTAGAATGTGAACC | 63893 |
| rs190698199 | snp | A/G | 5.43464e-05 | 0.00521251 | intron-variant | UBE2O | GRCh38.p7 | 17:76399959 | ACAGGGCTGTGAGGT[A/G]CACCTGGGCAGGCCT | 63893 |
| rs190699962 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76440976 | AGTGCAGGGGGCACC[C/T]GTGTAGTCAGTGAAG | 63893 |
| rs190790579 | snp | C/T | 0.00993419 | 0.0697739 | intron-variant | UBE2O | GRCh38.p7 | 17:76427641 | GCAAGCAAGAAGCTT[C/T]AGGGGTATCGCCAGT | 63893 |
| rs190917904 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE2O | GRCh38.p7 | 17:76409662 | GCCTCCCAAAGTGCT[A/G]GGATTACAGGCGTGA | 63893 |
| rs190934658 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76422569 | GTGTCCGAGCAGGAC[A/G]GAGGTTCCATCTGCA | 63893 |
| rs190939535 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76394737 | GTGGGAAGAGGCCTA[C/T]GATTCGGGGAGAAAG | 63893 |
| rs191020192 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76442200 | TGCCTGGGGAGCCCG[C/T]GACGGAAGTTGCCAA | 63893 |
| rs191033162 | snp | C/T | | | intron-variant | UBE2O | GRCh38.p7 | 17:76447460 | TCATGACTGCTCTTA[C/T]TACCTTAAAATATAA | 63893 |
| rs191034360 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76418040 | ACCTCAGGAGGAAGG[C/T]GCAGGGGGAGGTCAC | 63893 |
| rs191117347 | snp | A/C/T | 0.00557542 | 0.0525036 | upstream-variant-2KB | AANAT, UBE2O | GRCh38.p7 | 17:76453332 | GGACGCTGAAGATGC[A/C/T]GCGGGGGGCGGGGGC | 63893 |
| rs191123201 | snp | A/G | 0.00119737 | 0.0244387 | intron-variant | UBE2O | GRCh38.p7 | 17:76434396 | GAAGGAAACCCCAAC[A/G]CGTAGGAAACACAGT | 63893 |
| rs191253452 | snp | A/G | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76414758 | TGGCAGGGGGCCAGC[A/G]GGCTGGTCTCTGCAG | 63893 |
| rs191290221 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76395327 | GCTGGGACTACAGGC[A/G]CCCGCATGGTGGCGG | 63893 |
| rs191296636 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE2O | GRCh38.p7 | 17:76437477 | AAAGAAAAAGAAAAA[A/G]AAAGGCAATTATGTT | 63893 |
| rs191366257 | snp | A/G | 0.0111196 | 0.0737302 | intron-variant | UBE2O | GRCh38.p7 | 17:76439248 | CTGTGCCTAGAACGC[A/G]GCAGGTGCCAACAAA | 63893 |
| rs191374935 | snp | A/G | | | intron-variant | UBE2O | GRCh38.p7 | 17:76429860 | GTCCAGCGTTACCCT[A/G]CCCCTTGCTCTGCCC | 63893 |
| rs191376946 | snp | A/T | 0.00279162 | 0.0372561 | intron-variant | UBE2O | GRCh38.p7 | 17:76408056 | AGGCTCTTGTGACTT[A/T]CCTTCCTAACTTCCT | 63893 |
| rs191485457 | snp | C/T | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76406274 | CCAAAAGCCCAGGCA[C/T]GTGATGCTCCCACCA | 63893 |
| rs191559497 | snp | C/T | 0.00199481 | 0.0315187 | intron-variant | UBE2O | GRCh38.p7 | 17:76446661 | ACTCAGCATTCCCAG[C/T]CGAAGGATGACAGCA | 63893 |
| rs191662472 | snp | A/G | 0.000399281 | 0.0141238 | intron-variant | UBE2O | GRCh38.p7 | 17:76407138 | CATGGCTGAGGTGGA[A/G]TCACCAAGGCAGCGG | 63893 |
| rs191748526 | snp | C/T | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76427227 | TCTAACTAACTTCTG[C/T]AGATCTGTTTTCCAG | 63893 |
| rs191848986 | snp | A/G | 0.00358779 | 0.0422022 | intron-variant | UBE2O | GRCh38.p7 | 17:76423626 | TGAACCTGGGAGGCG[A/G]AGCTTGCAGTGAGCC | 63893 |
| rs191856671 | snp | C/T | 0.00119737 | 0.0244387 | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76451368 | AATTTTCCTTCCAAG[C/T]CTCAGAGCTGTTGCC | 63893 |
| rs191885174 | snp | C/T | 0.000798403 | 0.0199641 | intron-variant | UBE2O | GRCh38.p7 | 17:76428893 | AAGGGTAGAGGGGAC[C/T]CCTCTACTATTTTTT | 63893 |
| rs191887743 | snp | C/G/T | 0.00358891 | 0.0422285 | upstream-variant-2KB, intron-variant | AANAT, UBE2O | GRCh38.p7 | 17:76452100 | GTCAGAATCCTCCCC[C/G/T]CCAAGTACTATTCAT | 63893 |
| rs191897338 | snp | A/G | 0.00159617 | 0.0282053 | intron-variant | UBE2O | GRCh38.p7 | 17:76448677 | AAACGCTTTGCCTCC[A/G]AAACGAAGGCTGAAC | 63893 |
| rs192135883 | snp | A/G | 0.00318978 | 0.0398085 | intron-variant | UBE2O | GRCh38.p7 | 17:76402204 | GATTCTGAGATGCCA[A/G]TGCGCCCACATGCCC | 63893 |
| rs192143720 | snp | C/T | 0.00279162 | 0.0372561 | intron-variant | UBE2O | GRCh38.p7 | 17:76432285 | TTATCAAAGTATGTT[C/T]CTGTCAATCCACAAA | 63893 |